메뉴 건너뛰기




Volumn , Issue , 2013, Pages 1-294

Alkynes in cycloadditions

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLENE; AROMATIZATION; BENZENE REFINING; HYDROCARBONS; LIGHTING; NAPHTHALENE; NONLINEAR OPTICS; ORGANOMETALLICS; PHOTONIC DEVICES; REGIOSELECTIVITY; SYNTHESIS (CHEMICAL);

EID: 85026260241     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1002/9781118709313     Document Type: Book
Times cited : (19)

References (489)
  • 1
    • 84977693045 scopus 로고
    • Cyclisierende polymerisation von acetylen III. Benzol, benzolderivate und hydroaromatische Verbindungen
    • Reppe, W. and Schweckendiek, W.J. (1948) Cyclisierende polymerisation von acetylen. III. Benzol, benzolderivate und hydroaromatische Verbindungen. Justus Liebigs Annalen der Chemie, 560(1), 104-116.
    • (1948) Justus Liebigs Annalen der Chemie , vol.560 , Issue.1 , pp. 104-116
    • Reppe, W.1    Schweckendiek, W.J.2
  • 2
    • 0347812067 scopus 로고    scopus 로고
    • Palladium-catalyzed benzannulation reactions of conjugated enynes and diynes
    • eds E. Negishi and de A. Meijere), John Wiley & Sons, New York
    • Saito, S. and Yamamoto, Y. (2002) Palladium-catalyzed benzannulation reactions of conjugated enynes and diynes, in Handbook of Organopalladium Chemistry for Organic Synthesis (eds E. Negishi and de A. Meijere), John Wiley & Sons, New York, p. 124.
    • (2002) Handbook of Organopalladium Chemistry for Organic Synthesis , pp. 124
    • Saito, S.1    Yamamoto, Y.2
  • 3
    • 0034250675 scopus 로고    scopus 로고
    • Recent advances in the transition-metalcatalyzed regioselective approaches to polysubstituted benzene derivatives
    • Saito, S. and Yamamoto, Y. (2000) Recent advances in the transition-metalcatalyzed regioselective approaches to polysubstituted benzene derivatives. Chemical Reviews, 100(8), 2901-2916.
    • (2000) Chemical Reviews , vol.100 , Issue.8 , pp. 2901-2916
    • Saito, S.1    Yamamoto, Y.2
  • 4
    • 2942557280 scopus 로고    scopus 로고
    • Transition-metal-catalyzed reactions in heterocyclic synthesis
    • (a) Nakamura, I. and Yamamoto, Y. (2004) Transition-metal-catalyzed reactions in heterocyclic synthesis. Chemical Reviews, 104(5), 2127-2198.
    • (2004) Chemical Reviews , vol.104 , Issue.5 , pp. 2127-2198
    • Nakamura, I.1    Yamamoto, Y.2
  • 5
    • 0002110351 scopus 로고    scopus 로고
    • Transition metal-mediated cycloaddition reactions
    • Lautens, M., Klute, W. and Tam, W. (1996) Transition metal-mediated cycloaddition reactions. Chemical Reviews, 96(1), 49-92.
    • (1996) Chemical Reviews , vol.96 , Issue.1 , pp. 49-92
    • Lautens, M.1    Klute, W.2    Tam, W.3
  • 6
    • 34548173261 scopus 로고    scopus 로고
    • Cationic rhodium (I)/BINAP-type bisphosphine complexes: versatile new catalysts for highly chemo-, regio-, and enantioselective [2+2+2] cycloadditions
    • Tanaka, K. (2007) Cationic rhodium (I)/BINAP-type bisphosphine complexes: versatile new catalysts for highly chemo-, regio-, and enantioselective [2+2+2] cycloadditions. Synlett, (13), 1977-1993.
    • (2007) Synlett , Issue.13 , pp. 1977-1993
    • Tanaka, K.1
  • 7
    • 34250653953 scopus 로고    scopus 로고
    • The fascinating construction of pyridine ring systems by transition metal-catalysed [2+2+2] cycloaddition reactions
    • Heller, B. and Hapke, M. (2007) The fascinating construction of pyridine ring systems by transition metal-catalysed [2+2+2] cycloaddition reactions. Chemical Society Reviews, 36(7), 1085-1094.
    • (2007) Chemical Society Reviews , vol.36 , Issue.7 , pp. 1085-1094
    • Heller, B.1    Hapke, M.2
  • 8
    • 80051586277 scopus 로고    scopus 로고
    • Cyclizations of alkynes: revisiting Baldwin's rules for ring closure
    • Gilmore, K. and Alabugin, I.V. (2011) Cyclizations of alkynes: revisiting Baldwin's rules for ring closure. Chemical Reviews, 111(11), 6513-6556.
    • (2011) Chemical Reviews , vol.111 , Issue.11 , pp. 6513-6556
    • Gilmore, K.1    Alabugin, I.V.2
  • 9
    • 83755207566 scopus 로고    scopus 로고
    • Acceleration of conjugated dienyne cycloaromatization
    • Hitt, D.M. and O'Connor, J.M. (2011) Acceleration of conjugated dienyne cycloaromatization. Chemical Reviews, 111(12), 7904-7922.
    • (2011) Chemical Reviews , vol.111 , Issue.12 , pp. 7904-7922
    • Hitt, D.M.1    O'Connor, J.M.2
  • 10
    • 70349782199 scopus 로고    scopus 로고
    • Beyond Reppe: building substituted arenes by [2+2+2] cycloadditions of alkynes
    • Galan, B.R. and Rovis, T. (2009) Beyond Reppe: building substituted arenes by [2+2+2] cycloadditions of alkynes. Angewandte Chemie International Edition, 48(16), 2830-2834.
    • (2009) Angewandte Chemie International Edition , vol.48 , Issue.16 , pp. 2830-2834
    • Galan, B.R.1    Rovis, T.2
  • 12
    • 33646589622 scopus 로고    scopus 로고
    • Dramatic acceleration of the Pd-catalyzed[4+2] benzannulation reaction of enynes and diynes in the presence of Lewis acids and bases expanded scope and new mechanistic insights
    • Rubina, M., Conley, M. and Gevorgyan, V. (2006) Dramatic acceleration of the Pd-catalyzed[4+2] benzannulation reaction of enynes and diynes in the presence of Lewis acids and bases expanded scope and new mechanistic insights. Journal of the American Chemical Society, 128(17), 5818-5827.
    • (2006) Journal of the American Chemical Society , vol.128 , Issue.17 , pp. 5818-5827
    • Rubina, M.1    Conley, M.2    Gevorgyan, V.3
  • 14
    • 0348010515 scopus 로고    scopus 로고
    • New advances in selected transition metal-catalyzed annulations
    • Rubin, M., Sromek, A. and Gevorgyan, V. (2003) New advances in selected transition metal-catalyzed annulations. Synlett, (15), 2265-2291.
    • (2003) Synlett , Issue.15 , pp. 2265-2291
    • Rubin, M.1    Sromek, A.2    Gevorgyan, V.3
  • 16
    • 85026210700 scopus 로고    scopus 로고
    • New data on the regioselective synthesis of aromatic structures based on acetylene-containing systems
    • Maretinam, I.A. (2008) New data on the regioselective synthesis of aromatic structures based on acetylene-containing systems. Processing of St. Petersburg Technological Institute (Tech. University), 3(29), 11-19.
    • (2008) Processing of St. Petersburg Technological Institute (Tech. University) , vol.3 , Issue.29 , pp. 11-19
    • Maretinam, I.A.1
  • 17
    • 33947088453 scopus 로고
    • p-Benzyne. Generation as an intermediate in a thermal isomerization reaction and trapping evidence for the 1, 4-benzenediyl structure
    • (a) Jones, R.R. and Bergmann, R.G. (1972) p-Benzyne. Generation as an intermediate in a thermal isomerization reaction and trapping evidence for the 1, 4-benzenediyl structure. Journal of the American Chemical Society, 94(2), 660-661.
    • (1972) Journal of the American Chemical Society , vol.94 , Issue.2 , pp. 660-661
    • Jones, R.R.1    Bergmann, R.G.2
  • 18
    • 84856211222 scopus 로고    scopus 로고
    • The Bergman cyclizations of the enediyne and its N-substituted analogs using multiconfigurational second-order perturbation theory
    • Dong, H., Chen, B.-Z. and Huang, M.B. (2012) The Bergman cyclizations of the enediyne and its N-substituted analogs using multiconfigurational second-order perturbation theory. Journal of Computational Chemistry, 33(5), 537-549.
    • (2012) Journal of Computational Chemistry , vol.33 , Issue.5 , pp. 537-549
    • Dong, H.1    Chen, B.-Z.2    Huang, M.B.3
  • 19
    • 0001380819 scopus 로고
    • Thermal generation of α,3-dehydrotoluene from (Z)-1, 2, 4-heptatrien-6-yne
    • Myers, A.G., Kuo, E.Y. and Finney, N.S. (1989) Thermal generation of α,3-dehydrotoluene from (Z)-1, 2, 4-heptatrien-6-yne. Journal of the American Chemical Society, 111(20), 8057-8059.
    • (1989) Journal of the American Chemical Society , vol.111 , Issue.20 , pp. 8057-8059
    • Myers, A.G.1    Kuo, E.Y.2    Finney, N.S.3
  • 20
    • 84857784454 scopus 로고    scopus 로고
    • 6 (Schmittel)/ ene cyclization of enyne-allenes-crossing the boundary between classical and nonstatistical kinetics
    • 6 (Schmittel)/ ene cyclization of enyne-allenes-crossing the boundary between classical and nonstatistical kinetics. Journal of Phisical Organic Chemistry, 25(3), 182-197.
    • (2012) Journal of Phisical Organic Chemistry , vol.25 , Issue.3 , pp. 182-197
    • Schmittel, M.1    Vavilala, C.2    Cinar, M.E.3
  • 21
    • 0002036041 scopus 로고
    • The enediyne antibiotics
    • eds P.J. Stang and F.L. Diederich), Marcel Dekker VCH, New York, Weinheim
    • Nicolaou, K.C. and Smith, A. (1995) The enediyne antibiotics, in Modern Acetylene Chemistry (eds P.J. Stang and F.L. Diederich), Marcel Dekker VCH, New York, Weinheim, p. 203.
    • (1995) Modern Acetylene Chemistry , pp. 203
    • Nicolaou, K.C.1    Smith, A.2
  • 24
    • 0000283004 scopus 로고    scopus 로고
    • DNA-damaging enediyne compounds
    • eds D.H.R. Barton, K. Nakanishi and O.Meth Cohn), Pergamon Press, New York
    • Xi, Z. and Goldberg, I.H. (1999) DNA-damaging enediyne compounds, in Comprehensive Natural Products Chemistry, vol. 7 (eds D.H.R. Barton, K. Nakanishi and O.Meth Cohn), Pergamon Press, New York, pp. 553-592.
    • (1999) Comprehensive Natural Products Chemistry , vol.7 , pp. 553-592
    • Xi, Z.1    Goldberg, I.H.2
  • 26
    • 0142200418 scopus 로고    scopus 로고
    • Chelation-controlled Bergman cyclization: synthesis and reactivity of enediynyl ligands
    • Basak, A., Mandal, S. and Bag, S.S. (2003) Chelation-controlled Bergman cyclization: synthesis and reactivity of enediynyl ligands. Chemical Reviews, 103(10), 4077-4094.
    • (2003) Chemical Reviews , vol.103 , Issue.10 , pp. 4077-4094
    • Basak, A.1    Mandal, S.2    Bag, S.S.3
  • 27
    • 84859039659 scopus 로고    scopus 로고
    • Recent developments in enediyne chemistry
    • Joshi, M.C. and Rawat, D.S. (2012) Recent developments in enediyne chemistry. Chemistry & Biodiversity, 9(3), 459-498.
    • (2012) Chemistry & Biodiversity , vol.9 , Issue.3 , pp. 459-498
    • Joshi, M.C.1    Rawat, D.S.2
  • 28
    • 42149170391 scopus 로고    scopus 로고
    • Enediyne antibiotics and their models: new prospects of acetylene chemistry
    • [Russian Chemical Reviews, 75(9), 825-845 (2006)]
    • Maretina, I.A. and Trofimov, B.A. (2006) Enediyne antibiotics and their models: new prospects of acetylene chemistry. Uspekhi Khimii, 75(9), 913-935 [Russian Chemical Reviews, 75(9), 825-845 (2006)].
    • (2006) Uspekhi Khimii , vol.75 , Issue.9 , pp. 913-935
    • Maretina, I.A.1    Trofimov, B.A.2
  • 29
    • 34547441348 scopus 로고    scopus 로고
    • Design, synthesis, and biological activity of unnatural enediynes and related analogues equipped with pH-dependent or phototriggering devices
    • Kar, M. and Basak, A. (2007) Design, synthesis, and biological activity of unnatural enediynes and related analogues equipped with pH-dependent or phototriggering devices. Chemical Reviews, 107(7), 2861-2890.
    • (2007) Chemical Reviews , vol.107 , Issue.7 , pp. 2861-2890
    • Kar, M.1    Basak, A.2
  • 30
    • 42149094975 scopus 로고    scopus 로고
    • Design strategy of enediynes and enyne-allenes
    • Maretina, I.A. (2008). Design strategy of enediynes and enyne-allenes. Russian Journal of General Chemistry, 78(2), 223-257.
    • (2008) Russian Journal of General Chemistry , vol.78 , Issue.2 , pp. 223-257
    • Maretina, I.A.1
  • 31
    • 70349642092 scopus 로고    scopus 로고
    • Porphyrin-ethynyl arrays: synthesis, design, and application
    • Maretina, I.A. (2009) Porphyrin-ethynyl arrays: synthesis, design, and application. Russian Journal of General Chemistry, 79(7), 1544-1581.
    • (2009) Russian Journal of General Chemistry , vol.79 , Issue.7 , pp. 1544-1581
    • Maretina, I.A.1
  • 32
    • 85026202448 scopus 로고    scopus 로고
    • Novel data on cycloaromatization of systems, containing (Z)-hex-3-en-1,5-diyne and (Z)-hepta-1,2,4-triene-6-yne units
    • ed. R.R. Kostikov), St. Petersburg University Press, St Petersburg, pp. 375-410 (Rus) (Eng).
    • Maretina, I.A. (2011) Novel data on cycloaromatization of systems, containing (Z)-hex-3-en-1,5-diyne and (Z)-hepta-1,2,4-triene-6-yne units, in Modern Problems of Organic Chemistry, (ed. R.R. Kostikov), St. Petersburg University Press, St Petersburg, pp. 375-410 (Rus), pp. 349-380 (Eng).
    • (2011) Modern Problems of Organic Chemistry , pp. 349-380
    • Maretina, I.A.1
  • 33
    • 70350676806 scopus 로고    scopus 로고
    • Which one is preferred: Myers-Saito cyclization of ene-yne-allene or Garratt-Braverman cyclization of conjugated bisallenic sulfone? A theoretical and experimental study
    • Basak, A., Das, S., Mallick, D. and Jemmis, D. (2009) Which one is preferred: Myers-Saito cyclization of ene-yne-allene or Garratt-Braverman cyclization of conjugated bisallenic sulfone? A theoretical and experimental study. Journal of the American Chemical Society, 131(43), 15695-15704.
    • (2009) Journal of the American Chemical Society , vol.131 , Issue.43 , pp. 15695-15704
    • Basak, A.1    Das, S.2    Mallick, D.3    Jemmis, D.4
  • 34
    • 0041723237 scopus 로고    scopus 로고
    • Diacetylene: industrially promising reactions
    • [Russian Chemical Reviews, 69(7), 591-608 (2000)]
    • Maretina, I.A. and Trofimov, B.A. (2000) Diacetylene: industrially promising reactions. Uspekhi Khimii, 69(7), 642-660 [Russian Chemical Reviews, 69(7), 591-608 (2000)].
    • (2000) Uspekhi Khimii , vol.69 , Issue.7 , pp. 642-660
    • Maretina, I.A.1    Trofimov, B.A.2
  • 35
    • 0036093441 scopus 로고    scopus 로고
    • Diacetylene and its derivatives in heterocyclization reactions
    • ed. A.R. Katritzky), Elsevier, New York, London
    • Maretina, I.A. and Trofimov, B.A. (2002) Diacetylene and its derivatives in heterocyclization reactions, in Advances in Heterocyclic Chemistry, vol. 82 (ed. A.R. Katritzky), Elsevier, New York, London, pp. 157-259.
    • (2002) Advances in Heterocyclic Chemistry , vol.82 , pp. 157-259
    • Maretina, I.A.1    Trofimov, B.A.2
  • 36
    • 79954457941 scopus 로고    scopus 로고
    • Synthesis of heterocycles via electrophilic cyclization of alkynes containing heteroatom
    • Godoi, B., Schumacher, R.F. and Zeni, G. (2011) Synthesis of heterocycles via electrophilic cyclization of alkynes containing heteroatom. Chemical Reviews, 111(4), 2937-2980. (b) Gulevskaya, A.V. and Tyaglivy, A.S. (2012) Nucleophilic cyclizations of enediynes as a method for polynuclear heterocycle synthesis. Chemistry of Heterocyclic Compounds, 48(1), 82-94.
    • (2011) Chemical Reviews , vol.111 , Issue.4 , pp. 2937-2980
    • Godoi, B.1    Schumacher, R.F.2    Zeni, G.3
  • 37
    • 84861227593 scopus 로고    scopus 로고
    • Nucleophilic cyclizations of enediynes as a method for polynuclear heterocycle synthesis
    • Gulevskaya, A.V. and Tyaglivy, A.S. (2012) Nucleophilic cyclizations of enediynes as a method for polynuclear heterocycle synthesis. Chemistry of Heterocyclic Compounds, 48(1), 82-94.
    • (2012) Chemistry of Heterocyclic Compounds , vol.48 , Issue.1 , pp. 82-94
    • Gulevskaya, A.V.1    Tyaglivy, A.S.2
  • 39
    • 0346432003 scopus 로고    scopus 로고
    • Synthesis of 1,1-diethoxybutan-3-one from industrial gases containing diacetylene
    • Maretina, I.A. and Tsil'ko, E. (2003) Synthesis of 1,1-diethoxybutan-3-one from industrial gases containing diacetylene. Khim. Prom., 80(11), 19-33.
    • (2003) Khim. Prom. , vol.80 , Issue.11 , pp. 19-33
    • Maretina, I.A.1    Tsil'ko, E.2
  • 40
    • 27544440645 scopus 로고    scopus 로고
    • Utilization of diacetylene in basic industrial organic synthesis
    • Maretina, I.A. (1996) Utilization of diacetylene in basic industrial organic synthesis. Russian Journal of Applied Chemistry, 69(3), 311-321.
    • (1996) Russian Journal of Applied Chemistry , vol.69 , Issue.3 , pp. 311-321
    • Maretina, I.A.1
  • 42
    • 0000134376 scopus 로고
    • Transition metal alkyne complexes: transition metal catalyzed cyclotrimerization
    • eds. E.W. Abel, F.G.A. Stone, G. Wilkinson, and L.S. Hegedus), Pergamon, Oxford
    • Grothahn, D.B. (1995) Transition metal alkyne complexes: transition metal catalyzed cyclotrimerization, in Comprehensive Organometallic Chemistry II, vol. 12 (eds. E.W. Abel, F.G.A. Stone, G. Wilkinson, and L.S. Hegedus), Pergamon, Oxford, pp. 741-770.
    • (1995) Comprehensive Organometallic Chemistry II , vol.12 , pp. 741-770
    • Grothahn, D.B.1
  • 43
    • 30744465624 scopus 로고    scopus 로고
    • Iridium complex-catalyzed [2+2+2] cycloaddition of α,ω-diynes with monoynes and monoenes
    • Kezuka, S., Tanaka, S., Ohe, T., Nakaya, Y. and Takeuchi, R. (2006) Iridium complex-catalyzed [2+2+2] cycloaddition of α,ω-diynes with monoynes and monoenes. Journal of Organic Chemistry, 71(2), 543-552.
    • (2006) Journal of Organic Chemistry , vol.71 , Issue.2 , pp. 543-552
    • Kezuka, S.1    Tanaka, S.2    Ohe, T.3    Nakaya, Y.4    Takeuchi, R.5
  • 44
    • 33645956545 scopus 로고    scopus 로고
    • A highly practical instant catalyst for cyclotrimerization of alkynes to substituted benzenes
    • Saino, N., Amemiya, F., Tanabe, E., Kase, K. and Okamoto, S. (2006) A highly practical instant catalyst for cyclotrimerization of alkynes to substituted benzenes. Organic Letters, 8(7), 1439-1442.
    • (2006) Organic Letters , vol.8 , Issue.7 , pp. 1439-1442
    • Saino, N.1    Amemiya, F.2    Tanabe, E.3    Kase, K.4    Okamoto, S.5
  • 45
    • 22244460188 scopus 로고    scopus 로고
    • Intramolecular cyclotrimerization of triynes catalyzed by N-heterocyclic carbene-CoCl2/Zn or -FeCl3/Zn
    • Saino, N., Kogure, D. and Okamoto, S. (2005) Intramolecular cyclotrimerization of triynes catalyzed by N-heterocyclic carbene-CoCl2/Zn or -FeCl3/Zn. Organic Letters, 7(14), 3065-3067.
    • (2005) Organic Letters , vol.7 , Issue.14 , pp. 3065-3067
    • Saino, N.1    Kogure, D.2    Okamoto, S.3
  • 46
    • 16444363706 scopus 로고    scopus 로고
    • A simple cobalt catalyst system for the efficient and regioselective cyclotrimerisation of alkynes
    • Hilt, G., Vogler, T., Hess, W. and Galbiati, F. (2005) A simple cobalt catalyst system for the efficient and regioselective cyclotrimerisation of alkynes. Journal of the Chemical Society, Chemical Communications, (11), 1474-1475.
    • (2005) Journal of the Chemical Society, Chemical Communications , Issue.11 , pp. 1474-1475
    • Hilt, G.1    Vogler, T.2    Hess, W.3    Galbiati, F.4
  • 47
    • 46849102032 scopus 로고    scopus 로고
    • Solvent-dependent regiochemical cyclotrimerisation of phenylacetylene with cobalt catalysts containing disulfide ligands: a case study
    • Hilt, G., Hengst, C. and Hess, W. (2008) Solvent-dependent regiochemical cyclotrimerisation of phenylacetylene with cobalt catalysts containing disulfide ligands: a case study. European Journal of Organic Chemistry, (13), 2293-2297.
    • (2008) European Journal of Organic Chemistry , Issue.13 , pp. 2293-2297
    • Hilt, G.1    Hengst, C.2    Hess, W.3
  • 48
    • 0346780615 scopus 로고    scopus 로고
    • Highly chemo-and regioselective intermolecular cyclotrimerization of alkynes catalyzed by cationic rhodium (I)/modified BINAP complexes
    • Tanaka, K. and Shirasaka, K. (2003) Highly chemo-and regioselective intermolecular cyclotrimerization of alkynes catalyzed by cationic rhodium (I)/modified BINAP complexes. Organic Letters, 5(24), 4697-4699.
    • (2003) Organic Letters , vol.5 , Issue.24 , pp. 4697-4699
    • Tanaka, K.1    Shirasaka, K.2
  • 49
    • 14544299221 scopus 로고    scopus 로고
    • Chemo-and regioselective intermolecular cyclotrimerization of terminal alkynes catalyzed by cationic rhodium (I)/modified BINAP complexes: application to onestep synthesis of paracyclophanes
    • Tanaka, K., Toyoda, K., Wada, A., Shirasaka, K. and Hirano, M. (2005) Chemo-and regioselective intermolecular cyclotrimerization of terminal alkynes catalyzed by cationic rhodium (I)/modified BINAP complexes: application to onestep synthesis of paracyclophanes. Chemistry-A European Journal, 11(4), 1145-1156.
    • (2005) Chemistry-A European Journal , vol.11 , Issue.4 , pp. 1145-1156
    • Tanaka, K.1    Toyoda, K.2    Wada, A.3    Shirasaka, K.4    Hirano, M.5
  • 50
    • 80054101180 scopus 로고    scopus 로고
    • Regioselective synthesis of 1,3,5-substituted benzenes via the InCl3/2-iodophenol-catalyzed cyclotrimerization of alkynes
    • Xu, Y.-I., Pan, Y., Wu, Q. Wang, H.S. and Liu, P.Z. (2011) Regioselective synthesis of 1,3,5-substituted benzenes via the InCl3/2-iodophenol-catalyzed cyclotrimerization of alkynes. Journal of Organic Chemistry, 76(20), 8472-8476.
    • (2011) Journal of Organic Chemistry , vol.76 , Issue.20 , pp. 8472-8476
    • Xu, Y.-I.1    Pan, Y.2    Wu, Q.3    Wang, H.S.4    Liu, P.Z.5
  • 51
    • 0035906507 scopus 로고    scopus 로고
    • CuCl2-induced regiospecifical synthesis of benzene derivatives in the palladium-catalyzed cyclotrimerization of alkynes
    • Li, J., Jiang, H. and Chen, M. (2001) CuCl2-induced regiospecifical synthesis of benzene derivatives in the palladium-catalyzed cyclotrimerization of alkynes. Journal of Organic Chemistry, 66(10), 3627-3629.
    • (2001) Journal of Organic Chemistry , vol.66 , Issue.10 , pp. 3627-3629
    • Li, J.1    Jiang, H.2    Chen, M.3
  • 52
    • 0034693339 scopus 로고    scopus 로고
    • Selective palladiumcatalyzed cocyclotrimerization of arynes with dimethyl acetylenedicarboxylate: a versatile method for the synthesis of polycyclic aromatic hydrocarbons
    • Peña, D., Pérez, D., Guitian, E. and Castedo, L. (2000) Selective palladiumcatalyzed cocyclotrimerization of arynes with dimethyl acetylenedicarboxylate: a versatile method for the synthesis of polycyclic aromatic hydrocarbons. Journal of Organic Chemistry, 65, 6944-6950.
    • (2000) Journal of Organic Chemistry , vol.65 , pp. 6944-6950
    • Peña, D.1    Pérez, D.2    Guitian, E.3    Castedo, L.4
  • 53
    • 0038671595 scopus 로고    scopus 로고
    • Synthesis of hexabenzotriphenylene and other strained polycyclic aromatic hydrocarbons by palladium-catalyzed cyclotrimerization of arynes
    • Peña, D., Pérez, D., Guitian, E. and Castedo, L. (1999) Synthesis of hexabenzotriphenylene and other strained polycyclic aromatic hydrocarbons by palladium-catalyzed cyclotrimerization of arynes. Organic Letters, 1(10), 1555-1557.
    • (1999) Organic Letters , vol.1 , Issue.10 , pp. 1555-1557
    • Peña, D.1    Pérez, D.2    Guitian, E.3    Castedo, L.4
  • 54
    • 0033549728 scopus 로고    scopus 로고
    • Rhodium (I)-catalyzed [2+2+2] cycloadditions with N-functionalized 1-alkynylamides: a conceptually new strategy for the regiospecific synthesis of substituted indolines
    • Witulski, B. and Stengel, T. (1999) Rhodium (I)-catalyzed [2+2+2] cycloadditions with N-functionalized 1-alkynylamides: a conceptually new strategy for the regiospecific synthesis of substituted indolines. Angewandte Chemie International Edition, 38(16), 2426-2430.
    • (1999) Angewandte Chemie International Edition , vol.38 , Issue.16 , pp. 2426-2430
    • Witulski, B.1    Stengel, T.2
  • 55
    • 0000830218 scopus 로고
    • Rhodium-catalyzed alkyne cyclotrimerization strategies for C-aryl glycoside synthesis
    • McDonald, F.E., Zhu, H.Y.H. and Holmquist, C.R. (1995) Rhodium-catalyzed alkyne cyclotrimerization strategies for C-aryl glycoside synthesis. Journal of the American Chemical Society, 117(24), 6605-6606.
    • (1995) Journal of the American Chemical Society , vol.117 , Issue.24 , pp. 6605-6606
    • McDonald, F.E.1    Zhu, H.Y.H.2    Holmquist, C.R.3
  • 56
    • 70749115763 scopus 로고    scopus 로고
    • Rhodium-catalyzed selective [2+2+2] cyclizations of 1,6-diynes with monoynes leading to isoindolines and isobenzofurans
    • Wu, W., Zhang, X.Y. and Kang, S.X. (2010) Rhodium-catalyzed selective [2+2+2] cyclizations of 1,6-diynes with monoynes leading to isoindolines and isobenzofurans. Chinese Chemical Letters, 21(1), 18-22.
    • (2010) Chinese Chemical Letters , vol.21 , Issue.1 , pp. 18-22
    • Wu, W.1    Zhang, X.Y.2    Kang, S.X.3
  • 57
    • 41549162312 scopus 로고    scopus 로고
    • Regioselective reductive opening of substituted phthalans: synthetic applications
    • Garcia, D., Foubelo, F. and Yus, M. (2008) Regioselective reductive opening of substituted phthalans: synthetic applications. Tetrahedron, 64(19), 4275-4286.
    • (2008) Tetrahedron , vol.64 , Issue.19 , pp. 4275-4286
    • Garcia, D.1    Foubelo, F.2    Yus, M.3
  • 58
    • 0037009049 scopus 로고    scopus 로고
    • A highly efficient and flexible synthesis of substituted carbazoles by rhodium-catalyzed inter-and intramolecular alkyne cyclotrimerizations
    • Witulski, B. and Alayrac, C. (2002) A highly efficient and flexible synthesis of substituted carbazoles by rhodium-catalyzed inter-and intramolecular alkyne cyclotrimerizations. Angewandte Chemie International Edition, 41(17), 3281-3284.
    • (2002) Angewandte Chemie International Edition , vol.41 , Issue.17 , pp. 3281-3284
    • Witulski, B.1    Alayrac, C.2
  • 59
    • 0002039004 scopus 로고
    • Cobaltacyclopentadiene complexes as starting materials in the synthesis of substituted benzenes, cyclohexadienes, thiophenes, selenophenes and pyrroles
    • Wakatsuki, Y., Kuramitsu, T. and Yamazaki, H. (1974) Cobaltacyclopentadiene complexes as starting materials in the synthesis of substituted benzenes, cyclohexadienes, thiophenes, selenophenes and pyrroles. Tetrahedron Letters, 15(51), 4549-4552.
    • (1974) Tetrahedron Letters , vol.15 , Issue.51 , pp. 4549-4552
    • Wakatsuki, Y.1    Kuramitsu, T.2    Yamazaki, H.3
  • 60
    • 84985571853 scopus 로고
    • Cobalt-mediated [2+2+2]-cycloadditions: a maturing synthetic strategy [new synthetic methods]
    • Vollhardt, K.P.C. (1984) Cobalt-mediated [2+2+2]-cycloadditions: a maturing synthetic strategy [new synthetic methods]. Angewandte Chemie (International Edition in English), 23(8), 539-556.
    • (1984) Angewandte Chemie (International Edition in English) , vol.23 , Issue.8 , pp. 539-556
    • Vollhardt, K.P.C.1
  • 61
    • 0028039221 scopus 로고
    • asymmetric synthesis of isoindoline and isoquinoline derivatives using nickel (0)-catalyzed [2+2+2]-cocyclization
    • Sato, Y., Nishimata, T. and Mori, M. (1994) asymmetric synthesis of isoindoline and isoquinoline derivatives using nickel (0)-catalyzed [2+2+2]-cocyclization. Journal of Organic Chemistry, 59(21), 6133-6135.
    • (1994) Journal of Organic Chemistry , vol.59 , Issue.21 , pp. 6133-6135
    • Sato, Y.1    Nishimata, T.2    Mori, M.3
  • 62
    • 0033525671 scopus 로고    scopus 로고
    • Transition metal catalysed synthesis of tetrahydro derivatives of [5]-, [6]-, and [7]helicene
    • Stara, I.G., Stary, I., Kollarovic, A., Teply, F., Vyskocil, S. and Saman, D. (1999) Transition metal catalysed synthesis of tetrahydro derivatives of [5]-, [6]-, and [7]helicene. Tetrahedron Letters, 40(10), 1993-1996.
    • (1999) Tetrahedron Letters , vol.40 , Issue.10 , pp. 1993-1996
    • Stara, I.G.1    Stary, I.2    Kollarovic, A.3    Teply, F.4    Vyskocil, S.5    Saman, D.6
  • 63
    • 4544286694 scopus 로고    scopus 로고
    • Cobalt(I)-catalyzed asymmetric [2+2+2] cycloaddition of alkynes and nitriles: synthesis of enantiomerically enriched atropoisomers of 2-arylpyridines
    • Gutnov, A., Heller, B., Fischer, C. et al. (2004) Cobalt(I)-catalyzed asymmetric [2+2+2] cycloaddition of alkynes and nitriles: synthesis of enantiomerically enriched atropoisomers of 2-arylpyridines. Angewandte Chemie International Edition, 43(29), 3795-3797.
    • (2004) Angewandte Chemie International Edition , vol.43 , Issue.29 , pp. 3795-3797
    • Gutnov, A.1    Heller, B.2    Fischer, C.3
  • 64
    • 3142763237 scopus 로고    scopus 로고
    • Iridium complexcatalyzed highly enantio-and diastereoselective [2+2+2] cycloaddition for the synthesis of axially chiral teraryl compounds
    • Shibata, T., Fujimoto, T., Yokota, K. and Takagi, K. (2004) Iridium complexcatalyzed highly enantio-and diastereoselective [2+2+2] cycloaddition for the synthesis of axially chiral teraryl compounds. Journal of the American Chemical Society, 126(27), 8382-8383.
    • (2004) Journal of the American Chemical Society , vol.126 , Issue.27 , pp. 8382-8383
    • Shibata, T.1    Fujimoto, T.2    Yokota, K.3    Takagi, K.4
  • 65
    • 11144315960 scopus 로고    scopus 로고
    • enantioselective synthesis of axially chiral phthalides through cationic [Rh(I)(H8-binap)]-catalyzed cross alkyne cyclotrimerization
    • Tanaka, K., Nishida, G., Wada, A. and Noguchi, K. (2004) enantioselective synthesis of axially chiral phthalides through cationic [Rh(I)(H8-binap)]-catalyzed cross alkyne cyclotrimerization. Angewandte Chemie International Edition, 43(47), 6510-6512.
    • (2004) Angewandte Chemie International Edition , vol.43 , Issue.47 , pp. 6510-6512
    • Tanaka, K.1    Nishida, G.2    Wada, A.3    Noguchi, K.4
  • 66
    • 41549116352 scopus 로고    scopus 로고
    • Recent advances in enantioselective [2+2+2] cycloaddition
    • Shibata, T. and Tsuchikama, K. (2008) Recent advances in enantioselective [2+2+2] cycloaddition. Organic & Biomolecular Chemistry, 6(8), 1317-1323.
    • (2008) Organic & Biomolecular Chemistry , vol.6 , Issue.8 , pp. 1317-1323
    • Shibata, T.1    Tsuchikama, K.2
  • 67
    • 33845270763 scopus 로고    scopus 로고
    • Iridium-catalyzed enantioselective [2+2+2] cycloaddition of diynes and monoalkynes for the generation of axial chiralities
    • Shibata, T., Arai, Y., Takami, K. et al. (2006) Iridium-catalyzed enantioselective [2+2+2] cycloaddition of diynes and monoalkynes for the generation of axial chiralities. Advanced Synthesis & Catalysis, 348(16-17), 2475-2483.
    • (2006) Advanced Synthesis & Catalysis , vol.348 , Issue.16-17 , pp. 2475-2483
    • Shibata, T.1    Arai, Y.2    Takami, K.3
  • 68
    • 37149017176 scopus 로고    scopus 로고
    • Iridiumcatalyzed consecutive and enantioselective [2+2+2] cycloaddition of tetraynes and hexaynes for the construction of an axially chiral biaryl system
    • Shibata, T., Yoshida, S., Arai, Y., Otsuka, M. and Endo, K. (2008) Iridiumcatalyzed consecutive and enantioselective [2+2+2] cycloaddition of tetraynes and hexaynes for the construction of an axially chiral biaryl system. Tetrahedron, 64(5), 821-830.
    • (2008) Tetrahedron , vol.64 , Issue.5 , pp. 821-830
    • Shibata, T.1    Yoshida, S.2    Arai, Y.3    Otsuka, M.4    Endo, K.5
  • 69
    • 84890619148 scopus 로고    scopus 로고
    • Rhodium (I)-catalyzed cycloisomerization and cyclotrimerization reactions
    • ed. P.A. Evans), Wiley-VCH, Weinheim
    • Fujiwara, M. and Ojima, I. (2005) Rhodium (I)-catalyzed cycloisomerization and cyclotrimerization reactions, in Modern Rhodium-Catalyzed Organic Reactions (ed. P.A. Evans), Wiley-VCH, Weinheim, pp. 129-149.
    • (2005) Modern Rhodium-Catalyzed Organic Reactions , pp. 129-149
    • Fujiwara, M.1    Ojima, I.2
  • 70
    • 33947244017 scopus 로고    scopus 로고
    • Catalytic [2+2+2] and thermal [4+2] cycloaddition of 1,2-bis(arylpropiolyl)benzenes
    • Tanaka, K., Suda, T., Noguchi, K. and Hirano, M. (2007) Catalytic [2+2+2] and thermal [4+2] cycloaddition of 1,2-bis(arylpropiolyl)benzenes. Journal of Organic Chemistry, 72(6), 2243-2246.
    • (2007) Journal of Organic Chemistry , vol.72 , Issue.6 , pp. 2243-2246
    • Tanaka, K.1    Suda, T.2    Noguchi, K.3    Hirano, M.4
  • 71
    • 33747221237 scopus 로고    scopus 로고
    • Enantioselective synthesis of tetra-ortho-substituted axially chiral biaryls through rhodium-catalyzed double [2+2+2] cycloaddition
    • Nishida, G., Suzuki, N., Noguchi, K. and Tanaka, K. (2006) Enantioselective synthesis of tetra-ortho-substituted axially chiral biaryls through rhodium-catalyzed double [2+2+2] cycloaddition. Organic Letters, 8(16), 3489-3492.
    • (2006) Organic Letters , vol.8 , Issue.16 , pp. 3489-3492
    • Nishida, G.1    Suzuki, N.2    Noguchi, K.3    Tanaka, K.4
  • 72
    • 33645856179 scopus 로고    scopus 로고
    • Enantioselective intramolecular [2+2+2] cycloaddition of triynes for the synthesis of atropisomeric chiral orthodiarylbenzene derivatives
    • Shibata, T., Tsuchikama, K. and Otsuka, M. (2006) Enantioselective intramolecular [2+2+2] cycloaddition of triynes for the synthesis of atropisomeric chiral orthodiarylbenzene derivatives. Tetrahedron: Asymmetry, 17(4), 614-619.
    • (2006) Tetrahedron: Asymmetry , vol.17 , Issue.4 , pp. 614-619
    • Shibata, T.1    Tsuchikama, K.2    Otsuka, M.3
  • 73
    • 29744448745 scopus 로고    scopus 로고
    • Ir-catalyzed almost perfect enantioselective synthesis of helical polyaryls based on an axially-chiral sequence
    • Shibata, T. and Tsuchikama, K. (2005) Ir-catalyzed almost perfect enantioselective synthesis of helical polyaryls based on an axially-chiral sequence. Journal of the Chemical Society, Chemical Communications, (48), 6017-6019.
    • (2005) Journal of the Chemical Society, Chemical Communications , Issue.48 , pp. 6017-6019
    • Shibata, T.1    Tsuchikama, K.2
  • 75
    • 34547938721 scopus 로고    scopus 로고
    • Enantioselective intramolecular [2+2+2] cycloaddition of enediynes for the synthesis of chiral cyclohexa-1,3-dienes
    • Shibata, T., Kurokawa, H. and Kanda, K. (2007) Enantioselective intramolecular [2+2+2] cycloaddition of enediynes for the synthesis of chiral cyclohexa-1,3-dienes. Journal of Organic Chemistry, 72(17), 6521-6525.
    • (2007) Journal of Organic Chemistry , vol.72 , Issue.17 , pp. 6521-6525
    • Shibata, T.1    Kurokawa, H.2    Kanda, K.3
  • 76
    • 34250727598 scopus 로고    scopus 로고
    • Enantioselective synthesis of C2-symmetric dimethyl cyclohexadienedicarboxylates through cationic rhodium(I)/modified-BINAP-catalyzed [2+2+2] cycloadditions
    • Tanaka, K., Nishida, G., Sagae, H. and Hirano, M. (2007) Enantioselective synthesis of C2-symmetric dimethyl cyclohexadienedicarboxylates through cationic rhodium(I)/modified-BINAP-catalyzed [2+2+2] cycloadditions. Synlett, (9), 1426-1430.
    • (2007) Synlett , Issue.9 , pp. 1426-1430
    • Tanaka, K.1    Nishida, G.2    Sagae, H.3    Hirano, M.4
  • 77
    • 17744371152 scopus 로고    scopus 로고
    • Synthesis of highly substituted indolines and indoles via intramolecular [4+2] cycloaddition of ynamides and conjugated enynes
    • Dunetz, J.R. and Danheiser, R.L. (2005) Synthesis of highly substituted indolines and indoles via intramolecular [4+2] cycloaddition of ynamides and conjugated enynes. Journal of the American Chemical Society, 127(16), 5776-5777.
    • (2005) Journal of the American Chemical Society , vol.127 , Issue.16 , pp. 5776-5777
    • Dunetz, J.R.1    Danheiser, R.L.2
  • 78
    • 31544442421 scopus 로고    scopus 로고
    • A ring-closing yne-carbonyl metathesis of ynamides
    • Kurtz, K.C.M., Hsung, R.P. and Zhang, Y. (2006) A ring-closing yne-carbonyl metathesis of ynamides. Organic Letters, 8(2), 231-234.
    • (2006) Organic Letters , vol.8 , Issue.2 , pp. 231-234
    • Kurtz, K.C.M.1    Hsung, R.P.2    Zhang, Y.3
  • 79
    • 33646053203 scopus 로고    scopus 로고
    • Enantioselective synthesis of axially chiral anilides through rhodium-catalyzed [2+2+2] cycloaddition of 1,6-diynes with trimethylsilylynamides
    • Tanaka, K., Takeishi, K. and Noguchi, K. (2006) Enantioselective synthesis of axially chiral anilides through rhodium-catalyzed [2+2+2] cycloaddition of 1,6-diynes with trimethylsilylynamides. Journal of the American Chemical Society, 128(14), 4586-4587.
    • (2006) Journal of the American Chemical Society , vol.128 , Issue.14 , pp. 4586-4587
    • Tanaka, K.1    Takeishi, K.2    Noguchi, K.3
  • 80
    • 33750485032 scopus 로고    scopus 로고
    • Rhodium(I)-catalyzed [2+2+2] cycloadditions of ynamides in the synthesis of amide-substituted chiral biaryls
    • Tracey, M.R., Oppenheimer, J. and Hsung, R.P. (2006) Rhodium(I)-catalyzed [2+2+2] cycloadditions of ynamides in the synthesis of amide-substituted chiral biaryls. Journal of Organic Chemistry, 71(22), 8629-8632.
    • (2006) Journal of Organic Chemistry , vol.71 , Issue.22 , pp. 8629-8632
    • Tracey, M.R.1    Oppenheimer, J.2    Hsung, R.P.3
  • 81
    • 0141677747 scopus 로고    scopus 로고
    • Construction of pyridine rings by metal-mediated [2+2+2] cycloaddition
    • Varela, J.A. and Saá, C. (2003) Construction of pyridine rings by metal-mediated [2+2+2] cycloaddition. Chemical Reviews, 103(9), 3787-3802.
    • (2003) Chemical Reviews , vol.103 , Issue.9 , pp. 3787-3802
    • Varela, J.A.1    Saá, C.2
  • 82
    • 0001680749 scopus 로고    scopus 로고
    • Synthesis of annelated substituted bipyridines and terpyridines by cobalt(I)-catalyzed [2+2+2] cycloaddition
    • Varela, J.A., Castedo, L. and Saa, C. (1997) Synthesis of annelated substituted bipyridines and terpyridines by cobalt(I)-catalyzed [2+2+2] cycloaddition. Journal of Organic Chemistry, 62(12), 4189-4192.
    • (1997) Journal of Organic Chemistry , vol.62 , Issue.12 , pp. 4189-4192
    • Varela, J.A.1    Castedo, L.2    Saa, C.3
  • 83
    • 33947147688 scopus 로고    scopus 로고
    • On-demand generation of an efficient catalyst for pyridine formation from unactivated nitriles and α,ω-diynes using CoCl2-6H2O, dppe, and Zn
    • Kase, K., Goswarmi, A., Ohtaki, K., Tanabe, E., Saino, N. and Okamoto, S. (2007) On-demand generation of an efficient catalyst for pyridine formation from unactivated nitriles and α,ω-diynes using CoCl2-6H2O, dppe, and Zn. Organic Letters, 9(5), 931-934.
    • (2007) Organic Letters , vol.9 , Issue.5 , pp. 931-934
    • Kase, K.1    Goswarmi, A.2    Ohtaki, K.3    Tanabe, E.4    Saino, N.5    Okamoto, S.6
  • 84
    • 33847058832 scopus 로고    scopus 로고
    • Synthesis of 5,6,7,8-tetrahydro-1,6-naphthyridines, and related heterocycles by cobalt-catalyzed [2+2+2] cyclizations
    • Zhou, Y., Porco, J.A. and Snyder, J.K. (2007) Synthesis of 5,6,7,8-tetrahydro-1,6-naphthyridines, and related heterocycles by cobalt-catalyzed [2+2+2] cyclizations. Organic Letters, 9(3), 393-396.
    • (2007) Organic Letters , vol.9 , Issue.3 , pp. 393-396
    • Zhou, Y.1    Porco, J.A.2    Snyder, J.K.3
  • 85
    • 0037453626 scopus 로고    scopus 로고
    • Synthesis of naturally occurring pyridine alkaloids via palladium-catalyzed coupling/migration chemistry
    • Wang, Y., Dong, X. and Larock, R.C. (2003) Synthesis of naturally occurring pyridine alkaloids via palladium-catalyzed coupling/migration chemistry. Journal of Organic Chemistry, 68(8), 3090-3098.
    • (2003) Journal of Organic Chemistry , vol.68 , Issue.8 , pp. 3090-3098
    • Wang, Y.1    Dong, X.2    Larock, R.C.3
  • 86
    • 0036056973 scopus 로고    scopus 로고
    • Biosynthesis inspired Diels-Alder route to pyridines: synthesis of the 2,3-dithiazolylpyridine core of the thiopeptide antibiotics
    • Moody, C.J., Hughes, R.A., Thompson, S.P. and Alcaraz, L. (2002) Biosynthesis inspired Diels-Alder route to pyridines: synthesis of the 2,3-dithiazolylpyridine core of the thiopeptide antibiotics. Journal of the Chemical Society, Chemical Communications, (16), 1760-1761.
    • (2002) Journal of the Chemical Society, Chemical Communications , Issue.16 , pp. 1760-1761
    • Moody, C.J.1    Hughes, R.A.2    Thompson, S.P.3    Alcaraz, L.4
  • 87
    • 0036456222 scopus 로고    scopus 로고
    • Total synthesis of the naturally occurring endothelin converting enzyme (ECE) inhibitor WS 75624 A
    • Bach, T. and Heuser, S. (2002) Total synthesis of the naturally occurring endothelin converting enzyme (ECE) inhibitor WS 75624 A. Synlett, (12), 2089-2091.
    • (2002) Synlett , Issue.12 , pp. 2089-2091
    • Bach, T.1    Heuser, S.2
  • 88
    • 33847030361 scopus 로고    scopus 로고
    • Cobalt-catalyzed intramolecular [2+2+2] cocyclotrimerization of nitrilediynes: an efficient route to tetra-and pentacyclic pyridine derivatives
    • Chang, H.T., Jeganmohan, M. and Cheng, Ch.-H. (2007) Cobalt-catalyzed intramolecular [2+2+2] cocyclotrimerization of nitrilediynes: an efficient route to tetra-and pentacyclic pyridine derivatives. Organic Letters, 9(3), 505-508.
    • (2007) Organic Letters , vol.9 , Issue.3 , pp. 505-508
    • Chang, H.T.1    Jeganmohan, M.2    Cheng, C.-H.3
  • 89
    • 0345686500 scopus 로고    scopus 로고
    • Facile and racemization-free conversion of chiral nitriles into pyridine derivatives
    • Heller, B., Sundermann, B., Fischer, C., et al. (2003) Facile and racemization-free conversion of chiral nitriles into pyridine derivatives. Journal of Organic Chemistry, 68(24), 9221-9225.
    • (2003) Journal of Organic Chemistry , vol.68 , Issue.24 , pp. 9221-9225
    • Heller, B.1    Sundermann, B.2    Fischer, C.3
  • 90
    • 38349138606 scopus 로고    scopus 로고
    • Synthesis of chiral pyridyl alcohols using a two-step catalytic approach
    • Heller, B., Redkin, D., Gutnov, A., et al. (2008) Synthesis of chiral pyridyl alcohols using a two-step catalytic approach. Synthesis-Stuttgart, (1), 69-74.
    • (2008) Synthesis-Stuttgart , Issue.1 , pp. 69-74
    • Heller, B.1    Redkin, D.2    Gutnov, A.3
  • 91
    • 77951108395 scopus 로고    scopus 로고
    • Intramolecular cobalt-catalyzed [2+2+2] cycloaddition of O-protected diyne-cyanohydrins
    • Meissner, A. and Groth, U. (2010) Intramolecular cobalt-catalyzed [2+2+2] cycloaddition of O-protected diyne-cyanohydrins. Synlett, (7), 1051-1054.
    • (2010) Synlett , Issue.7 , pp. 1051-1054
    • Meissner, A.1    Groth, U.2
  • 92
    • 84863337931 scopus 로고    scopus 로고
    • Helicenes: synthesis and applications
    • Shen, Y. and Chen, Ch.-F. (2012) Helicenes: synthesis and applications. Chemical Reviews, 112(3), 1463-1535.
    • (2012) Chemical Reviews , vol.112 , Issue.3 , pp. 1463-1535
    • Shen, Y.1    Chen, C.-F.2
  • 93
    • 27744553556 scopus 로고    scopus 로고
    • Asymmetric synthesis of [7]helicene-like molecules
    • Star á, I.G., Alexandrová, Z., Teplý, F., et al. (2005) Asymmetric synthesis of [7]helicene-like molecules. Organic Letters, 7(13), 2547-2550.
    • (2005) Organic Letters , vol.7 , Issue.13 , pp. 2547-2550
    • Stará, I.G.1    Alexandrová, Z.2    Teplý, F.3
  • 94
    • 41849127860 scopus 로고    scopus 로고
    • On the origin of diastereoselectivity in [2+2+2] cycloisomerization of chiral triynes: controlling helicity of helicenelike compounds by thermodynamic factors
    • Sehnal, P., Krausova, Z., Teply, F., et al. (2008) On the origin of diastereoselectivity in [2+2+2] cycloisomerization of chiral triynes: controlling helicity of helicenelike compounds by thermodynamic factors. Journal of Organic Chemistry, 73(6), 2074-2082.
    • (2008) Journal of Organic Chemistry , vol.73 , Issue.6 , pp. 2074-2082
    • Sehnal, P.1    Krausova, Z.2    Teply, F.3
  • 95
    • 70349932165 scopus 로고    scopus 로고
    • One-step construction of five successive rings by rhodium-catalyzed intermolecular double [2+2+2] cycloaddition: enantioenriched [9]helicene-like molecules
    • Tanaka, K., Fukawa, N., Suda, T. and Noguchi, K. (2009) One-step construction of five successive rings by rhodium-catalyzed intermolecular double [2+2+2] cycloaddition: enantioenriched [9]helicene-like molecules. Angewandte Chemie International Edition, 48(30), 5470-5473.
    • (2009) Angewandte Chemie International Edition , vol.48 , Issue.30 , pp. 5470-5473
    • Tanaka, K.1    Fukawa, N.2    Suda, T.3    Noguchi, K.4
  • 96
    • 35048851486 scopus 로고    scopus 로고
    • Rhcatalyzed synthesis of helically chiral and ladder-type molecules via [2+2+2] and formal [2+1+2+1] cycloadditions involving C=C triple bond cleavage
    • Tanaka, K., Kamisawa, A., Suda, T., Noguchi, K. and Hirano, M. (2007) Rhcatalyzed synthesis of helically chiral and ladder-type molecules via [2+2+2] and formal [2+1+2+1] cycloadditions involving C=C triple bond cleavage. Journal of the American Chemical Society, 129(40), 12078-12079.
    • (2007) Journal of the American Chemical Society , vol.129 , Issue.40 , pp. 12078-12079
    • Tanaka, K.1    Kamisawa, A.2    Suda, T.3    Noguchi, K.4    Hirano, M.5
  • 97
    • 84961979242 scopus 로고    scopus 로고
    • Synthesis of [5]-, [6]-, and [7] helicene via Ni(0)-or Co(I)-catalyzed isomerization of aromatic cis,cis-Dienetriynes
    • Teplý, F., Star á, I.G., Star ý, I., et al. (2002) Synthesis of [5]-, [6]-, and [7] helicene via Ni(0)-or Co(I)-catalyzed isomerization of aromatic cis,cis-Dienetriynes. Journal of the American Chemical Society, 124(31), 9175-9180.
    • (2002) Journal of the American Chemical Society , vol.124 , Issue.31 , pp. 9175-9180
    • Teplý, F.1    Stará, I.G.2    Starý, I.3
  • 98
    • 51049114227 scopus 로고    scopus 로고
    • A straightforward route to helically chiral N-heteroaromatic compounds: practical synthesis of racemic 1,14-diaza[5]helicene and optically pure 1-and 2-aza [6]helicenes
    • Misek, J., Teply, F., Stara, I.G., et al. (2008) A straightforward route to helically chiral N-heteroaromatic compounds: practical synthesis of racemic 1,14-diaza[5]helicene and optically pure 1-and 2-aza [6]helicenes. Angewandte Chemie International Edition, 47(17), 3188-3191.
    • (2008) Angewandte Chemie International Edition , vol.47 , Issue.17 , pp. 3188-3191
    • Misek, J.1    Teply, F.2    Stara, I.G.3
  • 99
    • 58449111504 scopus 로고    scopus 로고
    • Helquats: a facile, modular, scalable route to novel helical dications
    • Adriaenssens, L., Severa, L., Silova, T. et al. (2009), Helquats: a facile, modular, scalable route to novel helical dications. Chemistry-A European Journal, 15(5), 1072-1076.
    • (2009) Chemistry-A European Journal , vol.15 , Issue.5 , pp. 1072-1076
    • Adriaenssens, L.1    Severa, L.2    Silova, T.3
  • 100
    • 77950636718 scopus 로고    scopus 로고
    • Highly modular assembly of cationic helical scaffolds: rapid synthesis of diverse helquats via differential quaternization
    • Severa, L., Adriaenssens, L., Vávra, J., et al. (2010) Highly modular assembly of cationic helical scaffolds: rapid synthesis of diverse helquats via differential quaternization. Tetrahedron, 66(19), 3537-3552.
    • (2010) Tetrahedron , vol.66 , Issue.19 , pp. 3537-3552
    • Severa, L.1    Adriaenssens, L.2    Vávra, J.3
  • 101
    • 34547936388 scopus 로고    scopus 로고
    • A new approach to polycyclic azonia cations by ring-closing metathesis
    • Nunez, A., Cuadro, A.M., Alvarez-Builla, J. and Vaquero, J.J. (2007) A new approach to polycyclic azonia cations by ring-closing metathesis. Organic Letters, 9(16), 2977-2980.
    • (2007) Organic Letters , vol.9 , Issue.16 , pp. 2977-2980
    • Nunez, A.1    Cuadro, A.M.2    Alvarez-Builla, J.3    Vaquero, J.J.4
  • 102
    • 4644303351 scopus 로고    scopus 로고
    • Synthesis of fused arylboronic esters via cobalt(0)-mediated cycloaddition of alkynylboronates with α,ω-diynes
    • Gandom, V., Leca, D., Aechtner, T., Vollhardt, K.P., Malacria, M. and Aubert, C. (2004) Synthesis of fused arylboronic esters via cobalt(0)-mediated cycloaddition of alkynylboronates with α,ω-diynes. Organic Letters, 6(19), 3405-3407.
    • (2004) Organic Letters , vol.6 , Issue.19 , pp. 3405-3407
    • Gandom, V.1    Leca, D.2    Aechtner, T.3    Vollhardt, K.P.4    Malacria, M.5    Aubert, C.6
  • 104
    • 33846421611 scopus 로고    scopus 로고
    • Synthesis of silafluorenes by iridium-catalyzed [2+2+2] cycloaddition of silicon-bridged diynes with alkynes
    • Matsuda, T., Kadowaki, Sh., Goya, V. and Murakami, M. (2007) Synthesis of silafluorenes by iridium-catalyzed [2+2+2] cycloaddition of silicon-bridged diynes with alkynes. Organic Letters, 9(1), 133-136.
    • (2007) Organic Letters , vol.9 , Issue.1 , pp. 133-136
    • Matsuda, T.1    Kadowaki, Sh.2    Goya, V.3    Murakami, M.4
  • 105
    • 77749296114 scopus 로고    scopus 로고
    • 1-Alkynylphosphines and their derivatives as key starting materials in creating new phosphines
    • Kondoh, A., Yorimitsu, H. and Oshima, K. (2010) 1-Alkynylphosphines and their derivatives as key starting materials in creating new phosphines. Chemistry-An Asian Journal, 5(3), 398-409.
    • (2010) Chemistry-An Asian Journal , vol.5 , Issue.3 , pp. 398-409
    • Kondoh, A.1    Yorimitsu, H.2    Oshima, K.3
  • 106
    • 67650079001 scopus 로고    scopus 로고
    • Transition-metal-catalyzed enantioselective [2+2+2] cycloadditions for the synthesis of axially chiral biaryls
    • Tanaka, K. (2009) Transition-metal-catalyzed enantioselective [2+2+2] cycloadditions for the synthesis of axially chiral biaryls. Chemistry-An Asian Journal, 4(4), 508-518.
    • (2009) Chemistry-An Asian Journal , vol.4 , Issue.4 , pp. 508-518
    • Tanaka, K.1
  • 107
    • 54849413194 scopus 로고    scopus 로고
    • Synthesis of bulky arylphosphanes by rhodium-catalyzed formal [2+2+2] cycloaddition reaction and their use as ligands
    • Kobatake, T., Kondoh, A., Yoshida, S., Yorimitsu, H. Oshima, K. (2008) Synthesis of bulky arylphosphanes by rhodium-catalyzed formal [2+2+2] cycloaddition reaction and their use as ligands. Chemistry-An Asian Journal, 3(8-9), 1613-1619.
    • (2008) Chemistry-An Asian Journal , vol.3 , Issue.8-9 , pp. 1613-1619
    • Kobatake, T.1    Kondoh, A.2    Yoshida, S.3    Yorimitsu, H.4    Oshima, K.5
  • 108
    • 34250210543 scopus 로고    scopus 로고
    • Synthesis of bulky phosphines by rhodium-catalyzed formal [2+2+2] cycloaddition reactions of tethered diynes with 1-alkynylphosphine sulfides
    • Kondoh, A., Yorimitsu, H. and Oshima, K. (2007) Synthesis of bulky phosphines by rhodium-catalyzed formal [2+2+2] cycloaddition reactions of tethered diynes with 1-alkynylphosphine sulfides. Journal of the American Chemical Society, 129(22), 6996-6997.
    • (2007) Journal of the American Chemical Society , vol.129 , Issue.22 , pp. 6996-6997
    • Kondoh, A.1    Yorimitsu, H.2    Oshima, K.3
  • 109
    • 34250771917 scopus 로고    scopus 로고
    • Asymmetric assembly of aromatic rings to produce tetra-ortho-substituted axially chiral biaryl phosphorus compounds
    • Nishida, G., Noguchi, K., Hirano, M. and Tanaka, K. (2007) Asymmetric assembly of aromatic rings to produce tetra-ortho-substituted axially chiral biaryl phosphorus compounds. Angewandte Chemie International Edition, 46(21), 3951-3954.
    • (2007) Angewandte Chemie International Edition , vol.46 , Issue.21 , pp. 3951-3954
    • Nishida, G.1    Noguchi, K.2    Hirano, M.3    Tanaka, K.4
  • 110
    • 33846585041 scopus 로고    scopus 로고
    • Phosphorus-bearing axially chiral biaryls by catalytic asymmetric cross-cyclotrimerization and a first application in asymmetric hydrosilylation
    • Heller, B., Gutnov, A., Fischer, C., et al. (2007), Phosphorus-bearing axially chiral biaryls by catalytic asymmetric cross-cyclotrimerization and a first application in asymmetric hydrosilylation. Chemistry-A European Journal, 13(4), 1117-1128.
    • (2007) Chemistry-A European Journal , vol.13 , Issue.4 , pp. 1117-1128
    • Heller, B.1    Gutnov, A.2    Fischer, C.3
  • 111
    • 22544487819 scopus 로고    scopus 로고
    • Cobalt(I)-mediated intramolecular [2+2+2] cocyclizations of (methylenecyclopropyl) diynes as an easy access to cyclopropanated oligocycles
    • Schelper, M., Buisine, O., Kozhushkov, S., Aubert, C., de Meijere, A. and Malacria, M. (2005). Cobalt(I)-mediated intramolecular [2+2+2] cocyclizations of (methylenecyclopropyl) diynes as an easy access to cyclopropanated oligocycles. European Journal of Organic Chemistry (14), 3000-3007.
    • (2005) European Journal of Organic Chemistry , Issue.14 , pp. 3000-3007
    • Schelper, M.1    Buisine, O.2    Kozhushkov, S.3    Aubert, C.4    de Meijere, A.5    Malacria, M.6
  • 112
    • 36348951591 scopus 로고    scopus 로고
    • Rhodium-catalyzed double [2+2+2] cycloaddition of 1,4-bis (diphenylphosphinoyl)buta-1,3-diyne with tethered diynes: a modular, highly versatile single-pot synthesis of NU-BIPHEP biaryl diphosphines
    • Doherty, S., Knight, J.G., Smyth, C.H., Harrington, R.W. and Clegg, W. (2007) Rhodium-catalyzed double [2+2+2] cycloaddition of 1,4-bis (diphenylphosphinoyl)buta-1,3-diyne with tethered diynes: a modular, highly versatile single-pot synthesis of NU-BIPHEP biaryl diphosphines. Organic Letters, 9(23), 4925-4928.
    • (2007) Organic Letters , vol.9 , Issue.23 , pp. 4925-4928
    • Doherty, S.1    Knight, J.G.2    Smyth, C.H.3    Harrington, R.W.4    Clegg, W.5
  • 113
    • 54249097359 scopus 로고    scopus 로고
    • Highly enantioselective synthesis of pseudo-C2-symmetric axially chiral biaryl diphosphines via rhodium-catalyzed double [2+2+2] cycloaddition
    • Doherty, S., Smyth, C.H., Harrington, R.W. and Clegg, W. (2008) Highly enantioselective synthesis of pseudo-C2-symmetric axially chiral biaryl diphosphines via rhodium-catalyzed double [2+2+2] cycloaddition. Organometallics, 27(19), 4837-4840.
    • (2008) Organometallics , vol.27 , Issue.19 , pp. 4837-4840
    • Doherty, S.1    Smyth, C.H.2    Harrington, R.W.3    Clegg, W.4
  • 114
    • 54249109621 scopus 로고    scopus 로고
    • Practical enantioselective synthesis of axially chiral biaryl diphosphonates and dicarboxylates by cationic rhodium(I)/Segphos-catalyzed double [2+2+2] cycloaddition
    • Nishida, G., Ogaki, S., Yusa, Y. Yokozawa, T., Noguchi, K. and Tanaka, K. (2008) Practical enantioselective synthesis of axially chiral biaryl diphosphonates and dicarboxylates by cationic rhodium(I)/Segphos-catalyzed double [2+2+2] cycloaddition. Organic Letters, 10(13), 2849-2852.
    • (2008) Organic Letters , vol.10 , Issue.13 , pp. 2849-2852
    • Nishida, G.1    Ogaki, S.2    Yusa, Y.3    Yokozawa, T.4    Noguchi, K.5    Tanaka, K.6
  • 115
    • 49749142458 scopus 로고    scopus 로고
    • Enantioselective synthesis of P-stereogenic alkynylphosphine oxides by Rh-catalyzed [2+2+2] cycloaddition
    • Nishida, G., Noguchi, K., Hirano, M. and Tanaka, K. (2008) Enantioselective synthesis of P-stereogenic alkynylphosphine oxides by Rh-catalyzed [2+2+2] cycloaddition. Angewandte Chemie International Edition, 47(18), 3410-3413.
    • (2008) Angewandte Chemie International Edition , vol.47 , Issue.18 , pp. 3410-3413
    • Nishida, G.1    Noguchi, K.2    Hirano, M.3    Tanaka, K.4
  • 116
    • 0036828222 scopus 로고    scopus 로고
    • Highly regio-and chemoselective[2 + 2 +2] cycloaddition of electrondeficient diynes with allenes catalyzed by nickel complexes: a novel entry to polysubstituted benzene derivatives
    • Shanmugasundaram, M., Wu, M.-S., Jeganmohan, M., Huang, C.W. and Cheng, C.H. (2002) Highly regio-and chemoselective[2 + 2 +2] cycloaddition of electrondeficient diynes with allenes catalyzed by nickel complexes: a novel entry to polysubstituted benzene derivatives. Journal of Organic Chemistry, 67(22), 7724-7729.
    • (2002) Journal of Organic Chemistry , vol.67 , Issue.22 , pp. 7724-7729
    • Shanmugasundaram, M.1    Wu, M.-S.2    Jeganmohan, M.3    Huang, C.W.4    Cheng, C.H.5
  • 118
    • 0034630934 scopus 로고    scopus 로고
    • Ru(II)-catalyzed cycloadditions of 1,6-heptadiynes with alkenes: new synthetic potential of ruthenacyclopentatrienes as biscarbenoids in tandem cyclopropanation of bicycloalkenes and heteroatom-assisted cyclocotrimerization of 1,6-heptadiynes with heterocyclic alkenes
    • Yamamoto, Y., Kitahara, H., Ogawa, R., Kawaguchi, H., Tatsumi, K. and Itoh, K. (2000) Ru(II)-catalyzed cycloadditions of 1,6-heptadiynes with alkenes: new synthetic potential of ruthenacyclopentatrienes as biscarbenoids in tandem cyclopropanation of bicycloalkenes and heteroatom-assisted cyclocotrimerization of 1,6-heptadiynes with heterocyclic alkenes. Journal of the American Chemical Society, 122(18), 4310-4319.
    • (2000) Journal of the American Chemical Society , vol.122 , Issue.18 , pp. 4310-4319
    • Yamamoto, Y.1    Kitahara, H.2    Ogawa, R.3    Kawaguchi, H.4    Tatsumi, K.5    Itoh, K.6
  • 119
    • 0032567406 scopus 로고    scopus 로고
    • Cp.*Ru(cod)Clcatalyzed [2+2+2] cycloaddition of 1,6-heptadiynes with allylic ethers A decisive role of coordination to the ether oxygen atom
    • Yamamoto, Y., Kitahara, H., Ogawa, R. and Itoh, K. (1998) Cp.*Ru(cod)Clcatalyzed [2+2+2] cycloaddition of 1,6-heptadiynes with allylic ethers. A decisive role of coordination to the ether oxygen atom. Journal of Organic Chemistry, 63(26), 9610-9611.
    • (1998) Journal of Organic Chemistry , vol.63 , Issue.26 , pp. 9610-9611
    • Yamamoto, Y.1    Kitahara, H.2    Ogawa, R.3    Itoh, K.4
  • 120
    • 33750357709 scopus 로고    scopus 로고
    • Highly enantioselective construction of a chiral spirocyclic structure by the [2+2+2] cycloaddition of diynes and exo-methylene cyclic compounds
    • Tsuchikama, K., Kuwata, Y. and Shibata, T. (2006) Highly enantioselective construction of a chiral spirocyclic structure by the [2+2+2] cycloaddition of diynes and exo-methylene cyclic compounds. Journal of the American Chemical Society, 128(42), 13686-13687.
    • (2006) Journal of the American Chemical Society , vol.128 , Issue.42 , pp. 13686-13687
    • Tsuchikama, K.1    Kuwata, Y.2    Shibata, T.3
  • 121
    • 36148999821 scopus 로고    scopus 로고
    • Rhodium-catalyzed enantioselective [2+2+2] cycloaddition of diynes with unfunctionalized alkenes
    • Shibata, T., Kawachi, A., Ogawa, M., Kuwata, Y., Tsuchikama, K. and Endo, K. (2007) Rhodium-catalyzed enantioselective [2+2+2] cycloaddition of diynes with unfunctionalized alkenes. Tetrahedron, 63(52), 12853-12859.
    • (2007) Tetrahedron , vol.63 , Issue.52 , pp. 12853-12859
    • Shibata, T.1    Kawachi, A.2    Ogawa, M.3    Kuwata, Y.4    Tsuchikama, K.5    Endo, K.6
  • 123
    • 0034826606 scopus 로고    scopus 로고
    • Synthesis of pyridinecontaining macrocycles by cobalt-mediated trimerization of triply-bonded species
    • Moretto, A.F., Zhang, H.-C. and Maryanoff, B.E. (2001) Synthesis of pyridinecontaining macrocycles by cobalt-mediated trimerization of triply-bonded species. Journal of the American Chemical Society, 123(13), 3157-3158.
    • (2001) Journal of the American Chemical Society , vol.123 , Issue.13 , pp. 3157-3158
    • Moretto, A.F.1    Zhang, H.-C.2    Maryanoff, B.E.3
  • 124
    • 0034820132 scopus 로고    scopus 로고
    • Significant chemo-and regioselectivies in the Ru(II)-catalyzed [2+2+2] cycloaddition of 1,6-diynes with dicyanides
    • Yamamoto, Y., Ogawa, R. and Itoh, K. (2001) Significant chemo-and regioselectivies in the Ru(II)-catalyzed [2+2+2] cycloaddition of 1,6-diynes with dicyanides. Journal of the American Chemical Society, 123(25), 6189-6190.
    • (2001) Journal of the American Chemical Society , vol.123 , Issue.25 , pp. 6189-6190
    • Yamamoto, Y.1    Ogawa, R.2    Itoh, K.3
  • 125
    • 0035927877 scopus 로고    scopus 로고
    • Ruthenium(II)-catalyzed [2+2+2] cycloaddition of 1,6-diynes with electron-deficient nitriles
    • Yamamoto, Y., Okuda, S. and Itoh, K. (2001) Ruthenium(II)-catalyzed [2+2+2] cycloaddition of 1,6-diynes with electron-deficient nitriles. Journal of the Chemical Society, Chemical Communications, (12), 1102-1103.
    • (2001) Journal of the Chemical Society, Chemical Communications , Issue.12 , pp. 1102-1103
    • Yamamoto, Y.1    Okuda, S.2    Itoh, K.3
  • 126
    • 0037134815 scopus 로고    scopus 로고
    • Ruthenium(II)-catalyzed [2+2+2] cycloaddition of 1,6-diynes with tricarbonyl compounds
    • Yamamoto, Y., Takagishi, H. and Itoh, K. (2002) Ruthenium(II)-catalyzed [2+2+2] cycloaddition of 1,6-diynes with tricarbonyl compounds. Journal of the American Chemical Society, 124(24), 6844-6845.
    • (2002) Journal of the American Chemical Society , vol.124 , Issue.24 , pp. 6844-6845
    • Yamamoto, Y.1    Takagishi, H.2    Itoh, K.3
  • 127
    • 0035802952 scopus 로고    scopus 로고
    • Regiocontrolled one-step synthesis of 3,3'-disubstituted 2,2'-bipyridine ligands by cobalt(I)-catalyzed cyclotrimerization
    • Varela, J.A., Castedo, L., Maestro, M., Mahia, J. and Saá, C. (2001) Regiocontrolled one-step synthesis of 3,3'-disubstituted 2,2'-bipyridine ligands by cobalt(I)-catalyzed cyclotrimerization. Chemistry-A European Journal, 7(23), 5203-5213.
    • (2001) Chemistry-A European Journal , vol.7 , Issue.23 , pp. 5203-5213
    • Varela, J.A.1    Castedo, L.2    Maestro, M.3    Mahia, J.4    Saá, C.5
  • 129
    • 0037045249 scopus 로고    scopus 로고
    • Ruthenium-catalyzed cycloaddition of 1,6-diynes with isothiocyanates and carbon disulfide: first transition-metal catalyzed [2+2+2] cocyclotrimerization involving C=S double bond
    • Yamamoto, Y., Takagishi, H. and Itoh, K. (2002) Ruthenium-catalyzed cycloaddition of 1,6-diynes with isothiocyanates and carbon disulfide: first transition-metal catalyzed [2+2+2] cocyclotrimerization involving C=S double bond. Journal of the American Chemical Society, 124(1), 28-29.
    • (2002) Journal of the American Chemical Society , vol.124 , Issue.1 , pp. 28-29
    • Yamamoto, Y.1    Takagishi, H.2    Itoh, K.3
  • 130
    • 33644961738 scopus 로고    scopus 로고
    • Rhodium-catalyzed [2+2+2] cycloaddition of 1,6-diynes with isothiocyanates and carbon disulfide
    • Tanaka, K., Wada, A. and Noguchi, K. (2006) Rhodium-catalyzed [2+2+2] cycloaddition of 1,6-diynes with isothiocyanates and carbon disulfide. Organic Letters, 8(5), 907-909.
    • (2006) Organic Letters , vol.8 , Issue.5 , pp. 907-909
    • Tanaka, K.1    Wada, A.2    Noguchi, K.3
  • 132
    • 13444292181 scopus 로고    scopus 로고
    • Pd-catalyzed one-pot multicomponent coupling reaction for the highly regioselective synthesis of polysubstituted benzenes
    • Xi, C., Chen, C., Ling, J. and Hong, X. (2005) Pd-catalyzed one-pot multicomponent coupling reaction for the highly regioselective synthesis of polysubstituted benzenes. Organic Letters, 7(2), 347-349.
    • (2005) Organic Letters , vol.7 , Issue.2 , pp. 347-349
    • Xi, C.1    Chen, C.2    Ling, J.3    Hong, X.4
  • 133
    • 10044289300 scopus 로고    scopus 로고
    • Stannylative cycloaddition of enynes catalyzed by palladium-iminophosphine
    • Nakao, Y., Hirata, Y., Ishihara, S. et al. (2004) Stannylative cycloaddition of enynes catalyzed by palladium-iminophosphine. Journal of the American Chemical Society, 126(48), 15650-15651.
    • (2004) Journal of the American Chemical Society , vol.126 , Issue.48 , pp. 15650-15651
    • Nakao, Y.1    Hirata, Y.2    Ishihara, S.3
  • 134
    • 0000433431 scopus 로고    scopus 로고
    • An efficient route to 2,6-disubstituted styrenes via the palladium-catalyzed [4+2] cyclodimerization of conjugated enynes
    • Gevorgyan, V., Tando, K., Uchiyama, N. and Yamamoto, Y. (1998) An efficient route to 2,6-disubstituted styrenes via the palladium-catalyzed [4+2] cyclodimerization of conjugated enynes. Journal of Organic Chemistry, 63(20), 7022-7025.
    • (1998) Journal of Organic Chemistry , vol.63 , Issue.20 , pp. 7022-7025
    • Gevorgyan, V.1    Tando, K.2    Uchiyama, N.3    Yamamoto, Y.4
  • 135
    • 0001266390 scopus 로고    scopus 로고
    • Regiospecific synthesis of polysubstituted phenols via the palladium-catalyzed enyne-diyne [4+2] crossbenzannulation pathway
    • Gevorgyan, V., Quan, L.G. and Yamamoto, Y. (1998) Regiospecific synthesis of polysubstituted phenols via the palladium-catalyzed enyne-diyne [4+2] crossbenzannulation pathway. Journal of Organic Chemistry, 63(4), 1244-1247.
    • (1998) Journal of Organic Chemistry , vol.63 , Issue.4 , pp. 1244-1247
    • Gevorgyan, V.1    Quan, L.G.2    Yamamoto, Y.3
  • 136
    • 0342632852 scopus 로고    scopus 로고
    • Effective synthesis of aryl ethers and coumaranones employing the palladium-catalyzed enyne-diyne [4+2] cycloaddition protocol
    • Gevorgyan, V., Quan, L.G. and Yamamoto, Y. (2000) Effective synthesis of aryl ethers and coumaranones employing the palladium-catalyzed enyne-diyne [4+2] cycloaddition protocol. Journal of Organic Chemistry, 65(2), 568-572.
    • (2000) Journal of Organic Chemistry , vol.65 , Issue.2 , pp. 568-572
    • Gevorgyan, V.1    Quan, L.G.2    Yamamoto, Y.3
  • 138
    • 0041529949 scopus 로고    scopus 로고
    • Highly regiocontrolled Pd-catalyzed cross-coupling reaction of terminal alkynes and allenylphosphine oxides
    • Rubin, M., Markov, J., Chuprakov, S., Wink, D.J and Gevorgyan, V. (2003) Highly regiocontrolled Pd-catalyzed cross-coupling reaction of terminal alkynes and allenylphosphine oxides. Journal of Organic Chemistry, 68(16), 6251-6256.
    • (2003) Journal of Organic Chemistry , vol.68 , Issue.16 , pp. 6251-6256
    • Rubin, M.1    Markov, J.2    Chuprakov, S.3    Wink, D.J.4    Gevorgyan, V.5
  • 139
    • 0035917338 scopus 로고    scopus 로고
    • Synthesis of cyclophanes via an intermolecular Pd-catalyzed enyne-diyne cross-benzannulation approach
    • Gevorgyan, V., Tsuboya, N. and Yamamoto, Y. (2001) Synthesis of cyclophanes via an intermolecular Pd-catalyzed enyne-diyne cross-benzannulation approach. Journal of Organic Chemistry, 66(8), 2743-2746.
    • (2001) Journal of Organic Chemistry , vol.66 , Issue.8 , pp. 2743-2746
    • Gevorgyan, V.1    Tsuboya, N.2    Yamamoto, Y.3
  • 140
    • 28744455778 scopus 로고    scopus 로고
    • Competitive 1,2-and 1,5-hydrogen shifts following 2-vinylbiphenyl photocyclization
    • Lewis, F.D., Sajimon, M.C., Zuo, X., Rubin, M. and Gevorgyan, V. (2005) Competitive 1,2-and 1,5-hydrogen shifts following 2-vinylbiphenyl photocyclization. Journal of Organic Chemistry, 70(25), 10447-10452.
    • (2005) Journal of Organic Chemistry , vol.70 , Issue.25 , pp. 10447-10452
    • Lewis, F.D.1    Sajimon, M.C.2    Zuo, X.3    Rubin, M.4    Gevorgyan, V.5
  • 141
    • 0030670480 scopus 로고    scopus 로고
    • First intermolecular regiospecific palladium-catalyzed enyne-diyne [4+2] cross-benzannulation reaction
    • Gevorgyan, V., Takeda, A. and Yamamoto, Y. (1997) First intermolecular regiospecific palladium-catalyzed enyne-diyne [4+2] cross-benzannulation reaction. Journal of the American Chemical Society, 119(46), 11313-11314.
    • (1997) Journal of the American Chemical Society , vol.119 , Issue.46 , pp. 11313-11314
    • Gevorgyan, V.1    Takeda, A.2    Yamamoto, Y.3
  • 142
    • 0001752763 scopus 로고    scopus 로고
    • Palladium-catalyzed enyne-yne [4+2] benzannulation as a new and general approach to polysubstituted benzenes
    • Gevorgyan, V. and Yamamoto, Y. (1999) Palladium-catalyzed enyne-yne [4+2] benzannulation as a new and general approach to polysubstituted benzenes. Journal of Organometallic Chemistry, 576(1-2), 232-247.
    • (1999) Journal of Organometallic Chemistry , vol.576 , Issue.1-2 , pp. 232-247
    • Gevorgyan, V.1    Yamamoto, Y.2
  • 144
    • 0030917961 scopus 로고    scopus 로고
    • Regioselective synthesis of 1,3,5-unsymmetrically substituted benzenes via the palladiumcatalyzed cyclotrimerization of 1,3-diynes
    • Takeda, A., Ohno, A., Kadota, I., Gevorgyan, V. and Yamamoto, Y. (1997) Regioselective synthesis of 1,3,5-unsymmetrically substituted benzenes via the palladiumcatalyzed cyclotrimerization of 1,3-diynes. Journal of the American Chemical Society, 119(19), 4547-4548.
    • (1997) Journal of the American Chemical Society , vol.119 , Issue.19 , pp. 4547-4548
    • Takeda, A.1    Ohno, A.2    Kadota, I.3    Gevorgyan, V.4    Yamamoto, Y.5
  • 145
    • 0031708442 scopus 로고    scopus 로고
    • Rhodium-catalyzed intermolecular [4+2] cycloaddition of unactivated substrates
    • Murakami, M., Ubukata, M., Itami, K. and Ito, Y. (1998) Rhodium-catalyzed intermolecular [4+2] cycloaddition of unactivated substrates. Angewandte Chemie International Edition, 37(16), 2248-2250.
    • (1998) Angewandte Chemie International Edition , vol.37 , Issue.16 , pp. 2248-2250
    • Murakami, M.1    Ubukata, M.2    Itami, K.3    Ito, Y.4
  • 146
    • 0141520554 scopus 로고    scopus 로고
    • "Formal" ruthenium-catalyzed [4+2+2] cycloaddition of 1,6-diynes to 1,3-dienes: formation of cyclooctatrienes vs vinylcyclohexadienes
    • Varela, J.A., Casteda, L. and Saá, C. (2003) "Formal" ruthenium-catalyzed [4+2+2] cycloaddition of 1,6-diynes to 1,3-dienes: formation of cyclooctatrienes vs vinylcyclohexadienes. Organic Letters, 5(17), 2841-2844.
    • (2003) Organic Letters , vol.5 , Issue.17 , pp. 2841-2844
    • Varela, J.A.1    Casteda, L.2    Saá, C.3
  • 147
    • 33644559029 scopus 로고    scopus 로고
    • Eight-membered ring construction by [4+2+2] annulation involving beta-carbon elimination
    • Murakami, M., Ashida, S. and Matsuda, T. (2006) Eight-membered ring construction by [4+2+2] annulation involving beta-carbon elimination. Journal of the American Chemical Society, 128(7), 2166-2167.
    • (2006) Journal of the American Chemical Society , vol.128 , Issue.7 , pp. 2166-2167
    • Murakami, M.1    Ashida, S.2    Matsuda, T.3
  • 148
  • 149
    • 17744383592 scopus 로고    scopus 로고
    • AuBr3-and Cu(OTf)2-catalyzed intramolecular [4+2] cycloaddition of tethered alkynyl and alkenyl enynones and enynals: a new synthetic method for functionalized polycyclic hydrocarbons
    • Asao, N., Sato, K., Menggenbateer and Yamamoto, Y. (2005) AuBr3-and Cu(OTf)2-catalyzed intramolecular [4+2] cycloaddition of tethered alkynyl and alkenyl enynones and enynals: a new synthetic method for functionalized polycyclic hydrocarbons. Journal of Organic Chemistry, 70(9), 3682-3685.
    • (2005) Journal of Organic Chemistry , vol.70 , Issue.9 , pp. 3682-3685
    • Asao, N.1    Sato, K.2    Menggenbateer.3    Yamamoto, Y.4
  • 151
    • 0036522941 scopus 로고    scopus 로고
    • The behavior of 1,n-enynes in the presence of transition metals
    • Aubert, C., Buisine, O. and Malacria, M. (2002) The behavior of 1,n-enynes in the presence of transition metals. Chemical Reviews, 102(3), 813-834.
    • (2002) Chemical Reviews , vol.102 , Issue.3 , pp. 813-834
    • Aubert, C.1    Buisine, O.2    Malacria, M.3
  • 152
    • 8744260648 scopus 로고    scopus 로고
    • Cobalt(I)-mediated [2+2+2] cyclization of allenediynes toward a diastereoselective approach to 11-aryl steroid skeletons
    • Petit, M., Aubert, C. and Malacria, M. (2004) Cobalt(I)-mediated [2+2+2] cyclization of allenediynes toward a diastereoselective approach to 11-aryl steroid skeletons. Organic Letters, 6(22), 3937-3940.
    • (2004) Organic Letters , vol.6 , Issue.22 , pp. 3937-3940
    • Petit, M.1    Aubert, C.2    Malacria, M.3
  • 153
    • 0030599225 scopus 로고    scopus 로고
    • First examples of cobaltmediated formal Alder ene reaction of allenynes
    • Lierena, D., Aubert, C. and Malakcria, M. (1996) First examples of cobaltmediated formal Alder ene reaction of allenynes. Tetrahedron Letters, 37(39), 7027-7030.
    • (1996) Tetrahedron Letters , vol.37 , Issue.39 , pp. 7027-7030
    • Lierena, D.1    Aubert, C.2    Malakcria, M.3
  • 154
    • 0032490981 scopus 로고    scopus 로고
    • Synthesis of variously substituted allenediynes and their cobalt (I)-mediated [2+2+2] cycloaddition reactions
    • Lierena, D., Buisine, O., Aubert, C. and Malakria, M. (1998) Synthesis of variously substituted allenediynes and their cobalt (I)-mediated [2+2+2] cycloaddition reactions. Tetrahedron, 54(32), 9373-9392.
    • (1998) Tetrahedron , vol.54 , Issue.32 , pp. 9373-9392
    • Lierena, D.1    Buisine, O.2    Aubert, C.3    Malakria, M.4
  • 155
    • 0033593556 scopus 로고    scopus 로고
    • Improvement of the cobaltmediated [2+2+2] cycloaddition of substituted linear enediynes
    • Slowinski, F., Aubert, C. and Malacria, M. (1999) Improvement of the cobaltmediated [2+2+2] cycloaddition of substituted linear enediynes. Tetrahedron Letters, 40(4), 707-710.
    • (1999) Tetrahedron Letters , vol.40 , Issue.4 , pp. 707-710
    • Slowinski, F.1    Aubert, C.2    Malacria, M.3
  • 156
    • 0033932188 scopus 로고    scopus 로고
    • First example of a total axial to centered chirality transfer in the [2+2+2] cycloadditions of allenediynes
    • Buisine, O., Aubert, C. and Malacria, M. (2000) First example of a total axial to centered chirality transfer in the [2+2+2] cycloadditions of allenediynes. Synthesis-Stuttgart, (7), 985-989.
    • (2000) Synthesis-Stuttgart , Issue.7 , pp. 985-989
    • Buisine, O.1    Aubert, C.2    Malacria, M.3
  • 157
    • 33645771783 scopus 로고    scopus 로고
    • Synthesis of (3S)-hydroxyandrosta-5,7-diene-17-ones via intramolecular cobalt-mediated [2+2+2] cycloaddition
    • Groth, U., Richter, N. and Kalogerakis, A. (2006) Synthesis of (3S)-hydroxyandrosta-5,7-diene-17-ones via intramolecular cobalt-mediated [2+2+2] cycloaddition. Synlett, (6), 905-908.
    • (2006) Synlett , Issue.6 , pp. 905-908
    • Groth, U.1    Richter, N.2    Kalogerakis, A.3
  • 158
    • 0000565561 scopus 로고    scopus 로고
    • New efficient construction of the ABC core of the taxoids via a sequence of consecutive cobalt(I)-mediated [2+2+2] and [4+2] cyclizations
    • Petit, M., Chouraqui, G., Phansavath, P., Aubert, C. and Malacria, M. (2002) New efficient construction of the ABC core of the taxoids via a sequence of consecutive cobalt(I)-mediated [2+2+2] and [4+2] cyclizations. Organic Letters, 4(6), 1027-1029.
    • (2002) Organic Letters , vol.4 , Issue.6 , pp. 1027-1029
    • Petit, M.1    Chouraqui, G.2    Phansavath, P.3    Aubert, C.4    Malacria, M.5
  • 159
    • 0344306305 scopus 로고    scopus 로고
    • [2+2+2]-cycloaddition of 4-hydroxy-substituted enediynes to 2-hydroxy-substituted decahydrophenanthrenes
    • Groth, U., Richter, N. and Kalogerakis, A. (2003) [2+2+2]-cycloaddition of 4-hydroxy-substituted enediynes to 2-hydroxy-substituted decahydrophenanthrenes. European Journal of Organic Chemistry, (23), 4634-4639.
    • (2003) European Journal of Organic Chemistry , Issue.23 , pp. 4634-4639
    • Groth, U.1    Richter, N.2    Kalogerakis, A.3
  • 160
    • 29444459761 scopus 로고    scopus 로고
    • Silicon-initiated carbonylative carbotricyclization and [2+2+2+1] cycloaddition of enediynes catalyzed by rhodium complexes
    • Bennacer, B., Fujiwara, M., Lee, S.-Y. and Ojima, I. (2005) Silicon-initiated carbonylative carbotricyclization and [2+2+2+1] cycloaddition of enediynes catalyzed by rhodium complexes. Journal of the American Chemical Society, 127(50), 17756-17767.
    • (2005) Journal of the American Chemical Society , vol.127 , Issue.50 , pp. 17756-17767
    • Bennacer, B.1    Fujiwara, M.2    Lee, S.-Y.3    Ojima, I.4
  • 161
    • 0037205927 scopus 로고    scopus 로고
    • Intermolecular transition metal-catalyzed [4+2+2] cycloaddition reactions: a new approach to the construction of eight-membered rings
    • Evans, P.A., Robinson, J.E., Baum, E.W. and Fazal, A.N. (2002) Intermolecular transition metal-catalyzed [4+2+2] cycloaddition reactions: a new approach to the construction of eight-membered rings. Journal of the American Chemical Society, 124(30), 8782-8783.
    • (2002) Journal of the American Chemical Society , vol.124 , Issue.30 , pp. 8782-8783
    • Evans, P.A.1    Robinson, J.E.2    Baum, E.W.3    Fazal, A.N.4
  • 162
    • 14844290896 scopus 로고    scopus 로고
    • Multicomponent cycloadditions: the four-component [5+1+2+1] cycloaddition of vinylcyclopropanes, alkynes, and CO
    • Wender, P.A., Gamber, G.G., Hubbard, R.D., Pham, S.M. and Zhang, L. (2005) Multicomponent cycloadditions: the four-component [5+1+2+1] cycloaddition of vinylcyclopropanes, alkynes, and CO. Journal of the American Chemical Society, 127(9), 2836-2837.
    • (2005) Journal of the American Chemical Society , vol.127 , Issue.9 , pp. 2836-2837
    • Wender, P.A.1    Gamber, G.G.2    Hubbard, R.D.3    Pham, S.M.4    Zhang, L.5
  • 163
    • 48849086704 scopus 로고    scopus 로고
    • Rhodium-catalyzed carbonylative [3+3+1] cycloaddition of biscyclopropanes with a vinyl substituent to form seven-membered rings
    • Kim, S.Y., Lee, S.I., Choi, S.Y. and Chung, Y.K. (2008) Rhodium-catalyzed carbonylative [3+3+1] cycloaddition of biscyclopropanes with a vinyl substituent to form seven-membered rings. Angewandte Chemie International Edition, 47(26), 4914-4917.
    • (2008) Angewandte Chemie International Edition , vol.47 , Issue.26 , pp. 4914-4917
    • Kim, S.Y.1    Lee, S.I.2    Choi, S.Y.3    Chung, Y.K.4
  • 164
    • 41549115473 scopus 로고    scopus 로고
    • Tandem Rh(I)-catalyzed [(5+2)+1] cycloaddition/ aldol reaction for the construction of linear triquinane skeleton: total syntheses of (±)-hirsutene and (±)-1-desoxyhypnophilin
    • Jiao, L., Yuan, C. and Yu, Z.-X. (2008) Tandem Rh(I)-catalyzed [(5+2)+1] cycloaddition/ aldol reaction for the construction of linear triquinane skeleton: total syntheses of (±)-hirsutene and (±)-1-desoxyhypnophilin. Journal of the American Chemical Society, 130(13), 4421-4430.
    • (2008) Journal of the American Chemical Society , vol.130 , Issue.13 , pp. 4421-4430
    • Jiao, L.1    Yuan, C.2    Yu, Z.-X.3
  • 165
    • 34548732383 scopus 로고    scopus 로고
    • Caribenols A and B, sea whip derived norditerpenes with novel tricarbocyclic skeletons
    • Wei, X., Rodriguez, I.I., Rodriguez, A.D. and Barnes, C.L. (2007) Caribenols A and B, sea whip derived norditerpenes with novel tricarbocyclic skeletons. Journal of Organic Chemistry, 72(19), 7386-7389.
    • (2007) Journal of Organic Chemistry , vol.72 , Issue.19 , pp. 7386-7389
    • Wei, X.1    Rodriguez, I.I.2    Rodriguez, A.D.3    Barnes, C.L.4
  • 166
    • 68149134781 scopus 로고    scopus 로고
    • One-step formation of fused tetracyclic skeletons from cyclohexene-diynes and carbon monoxide through Rh(I)-catalyzed [2+2+2+1] cycloaddition reaction
    • Kaloko, J.J., Teng, Y.-H.G. and Ojima, I. (2009) One-step formation of fused tetracyclic skeletons from cyclohexene-diynes and carbon monoxide through Rh(I)-catalyzed [2+2+2+1] cycloaddition reaction. Journal of the Chemical Society, Chemical Communications, (30), 4569-4571.
    • (2009) Journal of the Chemical Society, Chemical Communications , Issue.30 , pp. 4569-4571
    • Kaloko, J.J.1    Teng, Y.-H.G.2    Ojima, I.3
  • 167
    • 0034654496 scopus 로고    scopus 로고
    • Rhodium-catalyzed novel carbonylative carbotricyclization of enediynes
    • Ojima, I. and Lee, S.-Y. (2000) Rhodium-catalyzed novel carbonylative carbotricyclization of enediynes. Journal of the American Chemical Society, 122(10), 2385-2386.
    • (2000) Journal of the American Chemical Society , vol.122 , Issue.10 , pp. 2385-2386
    • Ojima, I.1    Lee, S.-Y.2
  • 168
    • 33846206028 scopus 로고    scopus 로고
    • Aromatic molecular-bowl hydrocarbons: synthetic derivatives, their structures, and physical properties
    • Wu, Y.-T. and Siegel, J.S. (2006) Aromatic molecular-bowl hydrocarbons: synthetic derivatives, their structures, and physical properties. Chemical Reviews, 106(12), 4843-4867.
    • (2006) Chemical Reviews , vol.106 , Issue.12 , pp. 4843-4867
    • Wu, Y.-T.1    Siegel, J.S.2
  • 171
    • 33744782312 scopus 로고    scopus 로고
    • Synthesis of fluoranthenes and indenocorannulenes: elucidation of chiral stereoisomers on the basis of static molecular bowls
    • Wu, Y.-T., Hayama, T., Baldrige, K.K. Linden, A. and Siegel, J.S. (2006) Synthesis of fluoranthenes and indenocorannulenes: elucidation of chiral stereoisomers on the basis of static molecular bowls. Journal of the American Chemical Society, 128(21), 6870-6884.
    • (2006) Journal of the American Chemical Society , vol.128 , Issue.21 , pp. 6870-6884
    • Wu, Y.-T.1    Hayama, T.2    Baldrige, K.K.3    Linden, A.4    Siegel, J.S.5
  • 172
    • 26444484255 scopus 로고    scopus 로고
    • Formal [(2+2)+2] and [(2+2)+(2+2)] nonconjugated dienediyne cascade cycloadditions
    • Wu, Y.T., Linden, A. and Siegel, J.S. (2005) Formal [(2+2)+2] and [(2+2)+(2+2)] nonconjugated dienediyne cascade cycloadditions. Organic Letters, 7(20), 4353-4355.
    • (2005) Organic Letters , vol.7 , Issue.20 , pp. 4353-4355
    • Wu, Y.T.1    Linden, A.2    Siegel, J.S.3
  • 173
    • 9344233880 scopus 로고    scopus 로고
    • Oligomers of hexa-peri-hexabenzocoronenes as "super-oligophenylenes": synthesis, electronic properties, and self-assembly
    • Wu, J., Watson, M.D., Tchebotareva, N., Wang, Z. and Müllen, K. (2004) Oligomers of hexa-peri-hexabenzocoronenes as "super-oligophenylenes": synthesis, electronic properties, and self-assembly. Journal of Organic Chemistry, 69(24), 8194-8201.
    • (2004) Journal of Organic Chemistry , vol.69 , Issue.24 , pp. 8194-8201
    • Wu, J.1    Watson, M.D.2    Tchebotareva, N.3    Wang, Z.4    Müllen, K.5
  • 174
    • 0037165720 scopus 로고    scopus 로고
    • Photoinduced electron-transfer processes along molecular wires based on phenylenevinylene oligomers: a quantum-chemical insight
    • Pourtois, G., Beljonne, D., Cornil, J., Ratner, M.A. and Bŕedas, J.L. (2002) Photoinduced electron-transfer processes along molecular wires based on phenylenevinylene oligomers: a quantum-chemical insight. Journal of the American Chemical Society, 124(16), 4436-4447.
    • (2002) Journal of the American Chemical Society , vol.124 , Issue.16 , pp. 4436-4447
    • Pourtois, G.1    Beljonne, D.2    Cornil, J.3    Ratner, M.A.4    Bŕedas, J.L.5
  • 175
    • 1642333104 scopus 로고    scopus 로고
    • Elaboration of diaryl ketones into naphthalenes fused on two or four sides: a naphthoannulation procedure
    • Donovan, P.M. and Scott, L.T. (2004) Elaboration of diaryl ketones into naphthalenes fused on two or four sides: a naphthoannulation procedure. Journal of the American Chemical Society, 126(10), 3108-3112.
    • (2004) Journal of the American Chemical Society , vol.126 , Issue.10 , pp. 3108-3112
    • Donovan, P.M.1    Scott, L.T.2
  • 176
    • 28144446216 scopus 로고    scopus 로고
    • Short and efficient synthesis of coronene derivatives via ruthenium-catalyzed benzannulation protocol
    • Shen, H.-Ch., Tang, J.-M., Chang, H.-K., Yang, C.W. and Liu, R.S. (2005) Short and efficient synthesis of coronene derivatives via ruthenium-catalyzed benzannulation protocol. Journal of Organic Chemistry, 70(24), 10113-10116.
    • (2005) Journal of Organic Chemistry , vol.70 , Issue.24 , pp. 10113-10116
    • Shen, H.-C.1    Tang, J.-M.2    Chang, H.-K.3    Yang, C.W.4    Liu, R.S.5
  • 178
    • 0037008980 scopus 로고    scopus 로고
    • Total syntheses and structures of angular [6]-and [7]phenylene: the first helical phenylenes (heliphenes)
    • Han, S., Bond, A.D., Disch, R.L., et al. (2002) Total syntheses and structures of angular [6]-and [7]phenylene: the first helical phenylenes (heliphenes). Angewandte Chemie International Edition, 41(17), 3223-3227.
    • (2002) Angewandte Chemie International Edition , vol.41 , Issue.17 , pp. 3223-3227
    • Han, S.1    Bond, A.D.2    Disch, R.L.3
  • 179
    • 0033559506 scopus 로고    scopus 로고
    • A novel phenylene topology: total syntheses of zigzag [4] and [5]phenylene
    • Eickmeier, C., Holmes, D., Junga, H., et al. (1999) A novel phenylene topology: total syntheses of zigzag [4] and [5]phenylene. Angewandte Chemie International Edition, 38(6), 800-804.
    • (1999) Angewandte Chemie International Edition , vol.38 , Issue.6 , pp. 800-804
    • Eickmeier, C.1    Holmes, D.2    Junga, H.3
  • 180
    • 33750491964 scopus 로고    scopus 로고
    • Revisit of the Dessy-White intramolecular acetylene-acetylene [2+2] cycloadditions
    • Lee, C.-C., Leung, M.K., Lee, G.-H., Liu, Y.H. and Peng, S.M. (2006) Revisit of the Dessy-White intramolecular acetylene-acetylene [2+2] cycloadditions. Journal of Organic Chemistry, 71(22), 8417-8423.
    • (2006) Journal of Organic Chemistry , vol.71 , Issue.22 , pp. 8417-8423
    • Lee, C.-C.1    Leung, M.K.2    Lee, G.-H.3    Liu, Y.H.4    Peng, S.M.5
  • 181
    • 0037009020 scopus 로고    scopus 로고
    • Total syntheses of angular [7]-, [8]-, and [9]phenylene by triple cobalt-catalyzed cycloisomerization: remarkably flexible heliphenes
    • Han, S., Anderson, D.R., Bond, A.D., et al. (2002) Total syntheses of angular [7]-, [8]-, and [9]phenylene by triple cobalt-catalyzed cycloisomerization: remarkably flexible heliphenes. Angewandte Chemie International Edition, 41(17), 3227-3230.
    • (2002) Angewandte Chemie International Edition , vol.41 , Issue.17 , pp. 3227-3230
    • Han, S.1    Anderson, D.R.2    Bond, A.D.3
  • 182
    • 0141786828 scopus 로고    scopus 로고
    • En route to archimedene: total synthesis of C3h-symmetric [7]phenylene
    • Bruns, D., Miura, H., Vollhardt, K.P.C. and Stanger, A. (2003) En route to archimedene: total synthesis of C3h-symmetric [7]phenylene. Organic Letters, 5(4), 549-552.
    • (2003) Organic Letters , vol.5 , Issue.4 , pp. 549-552
    • Bruns, D.1    Miura, H.2    Vollhardt, K.P.C.3    Stanger, A.4
  • 183
    • 24944503132 scopus 로고    scopus 로고
    • 1,3,6,9,12,14,17, 20-octaethynyltetrabenz-[a,b,f,j,k,o]-4,5,10,11,15,16,21,22-octadehydro[18]annul ene: a carbon-rich hydrocarbon
    • Miljanic, O.S., Holmes, D. and Vollhardt, K.P.C. (2005) 1,3,6,9,12,14,17, 20-octaethynyltetrabenz-[a,b,f,j,k,o]-4,5,10,11,15,16,21,22-octadehydro[18]annul ene: a carbon-rich hydrocarbon. Organic Letters, 7(8), 4001-4004.
    • (2005) Organic Letters , vol.7 , Issue.8 , pp. 4001-4004
    • Miljanic, O.S.1    Holmes, D.2    Vollhardt, K.P.C.3
  • 184
    • 78650630770 scopus 로고    scopus 로고
    • [2+2+2] cycloaddition reactions of macrocyclic systems catalyzed by transition metals
    • Pla-Quintana, A. and Roglans, A. (2010) [2+2+2] cycloaddition reactions of macrocyclic systems catalyzed by transition metals. Molecules, 15(12), 9230-9251.
    • (2010) Molecules , vol.15 , Issue.12 , pp. 9230-9251
    • Pla-Quintana, A.1    Roglans, A.2
  • 185
    • 0013654218 scopus 로고
    • 1,5,9-cyclododecatriyn Synthesis and conversion to intermediate 1,2:3,4:5,6-tricyclobutabenzene
    • Barkovich, A.J. and Vollhardt, K.P.C., (1976) 1,5,9-cyclododecatriyne. Synthesis and conversion to intermediate 1,2:3,4:5,6-tricyclobutabenzene. Journal of the American Chemical Society, 98(9), 2667-2668.
    • (1976) Journal of the American Chemical Society , vol.98 , Issue.9 , pp. 2667-2668
    • Barkovich, A.J.1    Vollhardt, K.P.C.2
  • 187
    • 0001255605 scopus 로고    scopus 로고
    • Novel φ-electron systems derived from silicon-containing macrocyclic polyacetylenes
    • Sakurai, H. (1996) Novel φ-electron systems derived from silicon-containing macrocyclic polyacetylenes. Pure and Applied Chemistry, 68(2), 327-333.
    • (1996) Pure and Applied Chemistry , vol.68 , Issue.2 , pp. 327-333
    • Sakurai, H.1
  • 188
    • 0002175061 scopus 로고    scopus 로고
    • Intramolecular oligomerization of disilalkylenes (-Me2Si(CH2)(n)SiMe2-)bridged cyclic triacetylenes
    • Ebata, K., Matsuo, T., Inoue, T., et al. (1996) Intramolecular oligomerization of disilalkylenes (-Me2Si(CH2)(n)SiMe2-)bridged cyclic triacetylenes. Chemistry Letters, 25(12), 1053-1054.
    • (1996) Chemistry Letters , vol.25 , Issue.12 , pp. 1053-1054
    • Ebata, K.1    Matsuo, T.2    Inoue, T.3
  • 189
    • 77950930734 scopus 로고    scopus 로고
    • Ene reactions between two alkynes? Doors open to thermally induced cycloisomerization of macrocyclic triynes and enediynes
    • Gonzalez, I., Pla-Quintana, A., Roglans, A., et al. (2010) Ene reactions between two alkynes? Doors open to thermally induced cycloisomerization of macrocyclic triynes and enediynes. Journal of the Chemical Society, Chemical Communications (46), 2944-2946.
    • (2010) Journal of the Chemical Society, Chemical Communications , Issue.46 , pp. 2944-2946
    • Gonzalez, I.1    Pla-Quintana, A.2    Roglans, A.3
  • 190
    • 52649170873 scopus 로고    scopus 로고
    • Fused tetracycles with a benzene or cyclohexadiene core: [2+2+2] cycloadditions on macrocyclic systems
    • Brun, S., Garcia, L., González, I. (2008) Fused tetracycles with a benzene or cyclohexadiene core: [2+2+2] cycloadditions on macrocyclic systems. Journal of the Chemical Society, Chemical Communications, (36), 4339-4341.
    • (2008) Journal of the Chemical Society, Chemical Communications , Issue.36 , pp. 4339-4341
    • Brun, S.1    Garcia, L.2    González, I.3
  • 191
    • 0037592751 scopus 로고    scopus 로고
    • Palladium(0)-catalyzed intramolecular [2+2+2] alkyne cyclotrimerizations with electron-deficient diynes and triynes
    • Yamamoto, Y., Nagata, A., Nagata, H., et al. (2003) Palladium(0)-catalyzed intramolecular [2+2+2] alkyne cyclotrimerizations with electron-deficient diynes and triynes. Chemistry-A European Journal, 9(11), 2469-2483.
    • (2003) Chemistry-A European Journal , vol.9 , Issue.11 , pp. 2469-2483
    • Yamamoto, Y.1    Nagata, A.2    Nagata, H.3
  • 193
    • 15444364555 scopus 로고    scopus 로고
    • Transition metal-mediated intramolecular [2+2+2] cycloisomerizations of cyclic triynes and enediynes
    • Torrent, A., Gonzalez, I., Pla-Quintana, A. and Roglans, A. (2005) Transition metal-mediated intramolecular [2+2+2] cycloisomerizations of cyclic triynes and enediynes. Journal of Organic Chemistry, 70(6), 2033-2041.
    • (2005) Journal of Organic Chemistry , vol.70 , Issue.6 , pp. 2033-2041
    • Torrent, A.1    Gonzalez, I.2    Pla-Quintana, A.3    Roglans, A.4
  • 194
    • 66249106713 scopus 로고    scopus 로고
    • Rhodium(I)-catalysed intramolecular [2+2+2] cyclotrimerisations of 15-, 20-and 25-membered azamacrocycles: experimental and theoretical mechanistic studies
    • Dachs, A., Torrent, A., Roglans, A., Parella, T, OsunaS. and Solà, M. (2009) Rhodium(I)-catalysed intramolecular [2+2+2] cyclotrimerisations of 15-, 20-and 25-membered azamacrocycles: experimental and theoretical mechanistic studies. Chemistry-A European Journal, 15(21), 5289-5300.
    • (2009) Chemistry-A European Journal , vol.15 , Issue.21 , pp. 5289-5300
    • Dachs, A.1    Torrent, A.2    Roglans, A.3    Parella, T.4    Osuna, S.5    Solà, M.6
  • 195
    • 34547842045 scopus 로고    scopus 로고
    • Palladium and rhodium-catalyzed intramolecular [2+2+2] cycloisomerizations in molten tetrabutylammonium bromide
    • Gonzalez, I., Bouquillon, S., Roglans, A. and Muzart, J. (2007) Palladium and rhodium-catalyzed intramolecular [2+2+2] cycloisomerizations in molten tetrabutylammonium bromide. Tetrahedron Letters, 48(37), 6425-6428.
    • (2007) Tetrahedron Letters , vol.48 , Issue.37 , pp. 6425-6428
    • Gonzalez, I.1    Bouquillon, S.2    Roglans, A.3    Muzart, J.4
  • 196
    • 70449441504 scopus 로고    scopus 로고
    • Rhodium N-heterocyclic carbene complexes as effective catalysts for [2+2+2] cycloaddition reactions
    • Gonzalez, I., Pla-Quintana, A. and Roglans, A. (2009) Rhodium N-heterocyclic carbene complexes as effective catalysts for [2+2+2] cycloaddition reactions. Synlett, (17), 2844-2848.
    • (2009) Synlett , Issue.17 , pp. 2844-2848
    • Gonzalez, I.1    Pla-Quintana, A.2    Roglans, A.3
  • 197
    • 77955584083 scopus 로고    scopus 로고
    • Formal [2+2+2] cycloaddition strategy based on an intramolecular propargylic ene reaction/Diels-Alder cycloaddition cascade
    • Robinson, J.M., Sakai, T., Okano, K., Kitawaki, T. and Danheiser, R.L. (2010) Formal [2+2+2] cycloaddition strategy based on an intramolecular propargylic ene reaction/Diels-Alder cycloaddition cascade. Journal of the American Chemical Society, 132(32), 11039-11041.
    • (2010) Journal of the American Chemical Society , vol.132 , Issue.32 , pp. 11039-11041
    • Robinson, J.M.1    Sakai, T.2    Okano, K.3    Kitawaki, T.4    Danheiser, R.L.5
  • 199
    • 0001582792 scopus 로고
    • 1,5,9-Tridehydro[l4]annulene and bicyclo[9.3.0]tetradeca-1,5,7,11,13-pentaene-3,9-diyne, an acetylenic homolog of azulene containing fused five-and eleven-membered rings
    • Mayer, J. and Sondheimer, F. (1966) 1,5,9-Tridehydro[l4]annulene and bicyclo[9.3.0]tetradeca-1,5,7,11,13-pentaene-3,9-diyne, an acetylenic homolog of azulene containing fused five-and eleven-membered rings. Journal of the American Chemical Society, 88(3), 602-603.
    • (1966) Journal of the American Chemical Society , vol.88 , Issue.3 , pp. 602-603
    • Mayer, J.1    Sondheimer, F.2
  • 200
    • 0000293837 scopus 로고
    • 5,12-Dihydro-6,11-didehydronaphthace A derivative of 1, 4-didehydronaphthalene
    • Wong, H.N. and Sondheimer, F., (1980) 5,12-Dihydro-6,11-didehydronaphthacene. A derivative of 1, 4-didehydronaphthalene. Tetrahedron Letters, 21(2), 217-220.
    • (1980) Tetrahedron Letters , vol.21 , Issue.2 , pp. 217-220
    • Wong, H.N.1    Sondheimer, F.2
  • 202
    • 0039218326 scopus 로고    scopus 로고
    • The art and science of organic and natural products synthesis
    • Nicolaou, K.C. and Winssinger, N. (1998) The art and science of organic and natural products synthesis. Journal of Chemical Education, 75(10), 1225-1258.
    • (1998) Journal of Chemical Education , vol.75 , Issue.10 , pp. 1225-1258
    • Nicolaou, K.C.1    Winssinger, N.2
  • 203
    • 0023689095 scopus 로고
    • Cyclic conjugated enediynes related to calicheamicins and esperamicins: calculations, synthesis, and properties
    • Nicolaou, K.C., Ogawa, Y., Zuccarello, G., Schweiger, E.J. and Kumazawa, T. (1988) Cyclic conjugated enediynes related to calicheamicins and esperamicins: calculations, synthesis, and properties. Journal of the American Chemical Society, 110(14), 4866-4868.
    • (1988) Journal of the American Chemical Society , vol.110 , Issue.14 , pp. 4866-4868
    • Nicolaou, K.C.1    Ogawa, Y.2    Zuccarello, G.3    Schweiger, E.J.4    Kumazawa, T.5
  • 204
    • 0000770422 scopus 로고    scopus 로고
    • Cascade radical cyclizations via biradicals generated from enediynes, enyne-allenes, and enyne-ketenes
    • Wang, K.K. (1996) Cascade radical cyclizations via biradicals generated from enediynes, enyne-allenes, and enyne-ketenes. Chemical Reviews, 96(1), 207-222.
    • (1996) Chemical Reviews , vol.96 , Issue.1 , pp. 207-222
    • Wang, K.K.1
  • 209
    • 0032517273 scopus 로고    scopus 로고
    • Synthesis of the antitumor agent aglycon (±)-calicheamicinone using an o-quinone monoketal strategy
    • Churcher, I., Hallett, D. and Magnus, P. (1998) Synthesis of the antitumor agent aglycon (±)-calicheamicinone using an o-quinone monoketal strategy. Journal of the American Chemical Society, 120(40), 10350-10358.
    • (1998) Journal of the American Chemical Society , vol.120 , Issue.40 , pp. 10350-10358
    • Churcher, I.1    Hallett, D.2    Magnus, P.3
  • 210
    • 0037087618 scopus 로고    scopus 로고
    • Enantioselective synthesis of kedarcidin chromophore aglycon in differentially protected form
    • Myers, A.G., Hogan, P.C., Hurd, A.R. and Goldberg, S.D. (2002) Enantioselective synthesis of kedarcidin chromophore aglycon in differentially protected form. Angewandte Chemie International Edition, 41(6), 1062-1064.
    • (2002) Angewandte Chemie International Edition , vol.41 , Issue.6 , pp. 1062-1064
    • Myers, A.G.1    Hogan, P.C.2    Hurd, A.R.3    Goldberg, S.D.4
  • 211
    • 0027952280 scopus 로고
    • On the DNA recognition role of the carbohydrate sector in calicheamicin: a comparison of DNA cleaving capacity of enantiomeric calicheamicinones
    • Aiyar, J., Hitchcock, S.A., Denhart, D., Liu, K.K.C., Danishefsky, S.J. and Crothers, D.M. (1994) On the DNA recognition role of the carbohydrate sector in calicheamicin: a comparison of DNA cleaving capacity of enantiomeric calicheamicinones. Angewandte Chemie International Edition, 33(8), 858-862.
    • (1994) Angewandte Chemie International Edition , vol.33 , Issue.8 , pp. 858-862
    • Aiyar, J.1    Hitchcock, S.A.2    Denhart, D.3    Liu, K.K.C.4    Danishefsky, S.J.5    Crothers, D.M.6
  • 213
    • 77950109576 scopus 로고    scopus 로고
    • Complexity and simplicity in the biosynthesis of enediyne natural products
    • Liang, Z.-X. (2010) Complexity and simplicity in the biosynthesis of enediyne natural products. Natural Product Reports, 27(4), 499-528.
    • (2010) Natural Product Reports , vol.27 , Issue.4 , pp. 499-528
    • Liang, Z.-X.1
  • 215
    • 6044276841 scopus 로고    scopus 로고
    • Spin trapping of 13C-labeled p-benzynes generated by Masamune-Bergman cyclization of bicyclic nine-membered enediynes
    • Usuki, T., Mita, T., Lear, M.J., et al. (2004) Spin trapping of 13C-labeled p-benzynes generated by Masamune-Bergman cyclization of bicyclic nine-membered enediynes. Angewandte Chemie International Edition, 43(39), 5249-5253.
    • (2004) Angewandte Chemie International Edition , vol.43 , Issue.39 , pp. 5249-5253
    • Usuki, T.1    Mita, T.2    Lear, M.J.3
  • 217
    • 0033971256 scopus 로고    scopus 로고
    • Paramagnetic enediyne antibiotic C-1027: spin identification and characterization of radical species
    • Hirama, M., Akijama, K., Tanaka, T., et al. (2000) Paramagnetic enediyne antibiotic C-1027: spin identification and characterization of radical species. Journal of the American Chemical Society, 122(4), 720-772.
    • (2000) Journal of the American Chemical Society , vol.122 , Issue.4 , pp. 720-772
    • Hirama, M.1    Akijama, K.2    Tanaka, T.3
  • 219
    • 0027175326 scopus 로고
    • Exclusive production of bistranded DNA damage by calicheamicin
    • Dedon, P.C., Salzberg, A.A. and Xu, J.H. (1993) Exclusive production of bistranded DNA damage by calicheamicin. Biochemistry, 32(14), 3617-3622.
    • (1993) Biochemistry , vol.32 , Issue.14 , pp. 3617-3622
    • Dedon, P.C.1    Salzberg, A.A.2    Xu, J.H.3
  • 221
    • 37549071843 scopus 로고    scopus 로고
    • Asymmetric synthesis and biological properties of uncialamycin and 26-epi-uncialamycin
    • Nicolaou, K.C., Chen, J.S., Zhang, H. and Montero, A. (2008) Asymmetric synthesis and biological properties of uncialamycin and 26-epi-uncialamycin. Angewandte Chemie International Edition, 47(1), 185-189.
    • (2008) Angewandte Chemie International Edition , vol.47 , Issue.1 , pp. 185-189
    • Nicolaou, K.C.1    Chen, J.S.2    Zhang, H.3    Montero, A.4
  • 223
    • 69549118838 scopus 로고    scopus 로고
    • Intramolecular imino Diels-Alder reaction: progress toward the synthesis of uncialamycin
    • Desrat, S. and van de Weghe, P. (2009) Intramolecular imino Diels-Alder reaction: progress toward the synthesis of uncialamycin. Journal of Organic Chemistry, 74(17), 6728-6734.
    • (2009) Journal of Organic Chemistry , vol.74 , Issue.17 , pp. 6728-6734
    • Desrat, S.1    van de Weghe, P.2
  • 224
    • 81155162606 scopus 로고    scopus 로고
    • Setbacks and hopes: en route to the synthesis of uncialamycin
    • Desrat, S., Jean, M. and van de Weghe, P. (2011) Setbacks and hopes: en route to the synthesis of uncialamycin. Tetrahedron, 67(39), 7510-7516.
    • (2011) Tetrahedron , vol.67 , Issue.39 , pp. 7510-7516
    • Desrat, S.1    Jean, M.2    van de Weghe, P.3
  • 225
    • 12344289470 scopus 로고    scopus 로고
    • Computational studies on the cyclizations of enediynes, enyne-allenes, and related polyunsaturated systems
    • Schreiner, P.R., Navarro-Vazquez, A. and Prall, M. (2005) Computational studies on the cyclizations of enediynes, enyne-allenes, and related polyunsaturated systems. Accounts of Chemical Research, 38(1), 29-37.
    • (2005) Accounts of Chemical Research , vol.38 , Issue.1 , pp. 29-37
    • Schreiner, P.R.1    Navarro-Vazquez, A.2    Prall, M.3
  • 226
    • 0035846423 scopus 로고    scopus 로고
    • Can fulvenes form from enediynes? A systematic highlevel computational study on parent and benzannelated enediyne and enyne-allene cyclizations
    • Prall, M., Wittkopp, A. and Schreiner, P.R. (2001) Can fulvenes form from enediynes? A systematic highlevel computational study on parent and benzannelated enediyne and enyne-allene cyclizations. Journal Physical Chemistry A, 105(40), 9265-9274.
    • (2001) Journal Physical Chemistry A , vol.105 , Issue.40 , pp. 9265-9274
    • Prall, M.1    Wittkopp, A.2    Schreiner, P.R.3
  • 227
    • 0030747770 scopus 로고    scopus 로고
    • The synthesis and reactivity of a novel 10-membered azaenediyne
    • Shain, J.C., Khamrai, U.K. and Basak, A. (1997) The synthesis and reactivity of a novel 10-membered azaenediyne. Tetrahedron Letters, 38(34), 6067-6070.
    • (1997) Tetrahedron Letters , vol.38 , Issue.34 , pp. 6067-6070
    • Shain, J.C.1    Khamrai, U.K.2    Basak, A.3
  • 231
    • 0028494263 scopus 로고
    • Experimental and theoretical studies of the mechanism and thermochemistry of formation of α,ndehydrotoluene biradicals from gas-phase halide elimination reactions
    • Wenthold, P.G., Wierschke, S.G., Nash, J.J. and Squires, R.R. (1994) Experimental and theoretical studies of the mechanism and thermochemistry of formation of α,ndehydrotoluene biradicals from gas-phase halide elimination reactions. Journal of the American Chemical Society, 116(16), 7378-7392.
    • (1994) Journal of the American Chemical Society , vol.116 , Issue.16 , pp. 7378-7392
    • Wenthold, P.G.1    Wierschke, S.G.2    Nash, J.J.3    Squires, R.R.4
  • 233
    • 5344278331 scopus 로고
    • Synthetic and mechanistic studies of esperamicin A1 and calicheamicin γ1-molecular strain rather than φ-bond proximity determines the cycloaromatization rates of bicycle[7,3,1] enediynes
    • Magnus, P., Fortt, S., Pitterna, T. and Snyder, J.P. (1990) Synthetic and mechanistic studies of esperamicin A1 and calicheamicin γ1-molecular strain rather than φ-bond proximity determines the cycloaromatization rates of bicycle[7,3,1] enediynes. Journal of the American Chemical Society, 112(12), 4986-4987.
    • (1990) Journal of the American Chemical Society , vol.112 , Issue.12 , pp. 4986-4987
    • Magnus, P.1    Fortt, S.2    Pitterna, T.3    Snyder, J.P.4
  • 234
    • 4644328562 scopus 로고    scopus 로고
    • Effect of remote trigonal carbons on the kinetics of Bergman cyclization: synthesis and chemical reactivity of pyridazinedione-based enediynes
    • Basak, A., Bag, S.S., Majumder, P.A., Das, A.K. and Bertolasi, V. (2004) Effect of remote trigonal carbons on the kinetics of Bergman cyclization: synthesis and chemical reactivity of pyridazinedione-based enediynes. Journal of Organic Chemistry, 69(20), 6927-6930.
    • (2004) Journal of Organic Chemistry , vol.69 , Issue.20 , pp. 6927-6930
    • Basak, A.1    Bag, S.S.2    Majumder, P.A.3    Das, A.K.4    Bertolasi, V.5
  • 235
    • 0032490113 scopus 로고    scopus 로고
    • Monocyclic enediynes: relationships between ring sizes, alkyne carbon distances, cyclization barriers, and hydrogen abstraction reactions
    • Schreiner, P.R. (1998) Monocyclic enediynes: relationships between ring sizes, alkyne carbon distances, cyclization barriers, and hydrogen abstraction reactions. Singlet-triplet separations of methyl-substituted p-benzynes. Journal of the American Chemical Society, 120(17), 4184-4190.
    • (1998) Singlet-triplet separations of methyl-substituted p-benzynes. Journal of the American Chemical Society , vol.120 , Issue.17 , pp. 4184-4190
    • Schreiner, P.R.1
  • 236
    • 0032514854 scopus 로고    scopus 로고
    • Rapid Bergman cyclization of 1,2-diethynylheteroarenes
    • Kim, C.-S. and Russell, K.C. (1998) Rapid Bergman cyclization of 1,2-diethynylheteroarenes. Journal of Organic Chemistry, 63(23), 8229-8234.
    • (1998) Journal of Organic Chemistry , vol.63 , Issue.23 , pp. 8229-8234
    • Kim, C.-S.1    Russell, K.C.2
  • 237
    • 0034596432 scopus 로고    scopus 로고
    • Linear free energy relationships in the Bergman cyclization of 4-substituted-1,2-diethynylbenzenes
    • Choy, N., Kim, C.-S., Ballestero, C., et al. (2000) Linear free energy relationships in the Bergman cyclization of 4-substituted-1,2-diethynylbenzenes. Tetrahedron Letters, 41(36), 6955-6958.
    • (2000) Tetrahedron Letters , vol.41 , Issue.36 , pp. 6955-6958
    • Choy, N.1    Kim, C.-S.2    Ballestero, C.3
  • 238
    • 0142030505 scopus 로고    scopus 로고
    • Synthesis and reactivity of enediynyl amino acids and peptides: a novel concept in lowering the activation energy of Bergman cyclisation by H-bonding and electrostatic interactions
    • Basak, A., Bag, S.S. and Bdour, H.M.M. (2003) Synthesis and reactivity of enediynyl amino acids and peptides: a novel concept in lowering the activation energy of Bergman cyclisation by H-bonding and electrostatic interactions. Journal of the Chemical Society, Chemical Communications, (20), 2614-2615.
    • (2003) Journal of the Chemical Society, Chemical Communications , Issue.20 , pp. 2614-2615
    • Basak, A.1    Bag, S.S.2    Bdour, H.M.M.3
  • 239
    • 0034810840 scopus 로고    scopus 로고
    • Electronic control of the Bergman cyclization: the remarkable role of vinyl substitution
    • Jones, G.B. and Warner, P.M. (2001) Electronic control of the Bergman cyclization: the remarkable role of vinyl substitution. Journal of the American Chemical Society, 123(10), 2134-2145.
    • (2001) Journal of the American Chemical Society , vol.123 , Issue.10 , pp. 2134-2145
    • Jones, G.B.1    Warner, P.M.2
  • 240
    • 0037018449 scopus 로고    scopus 로고
    • Tuning rate of the Bergman cyclization of benzannelated enediynes with ortho substituents
    • Alabugin, I.V., Manoharan, M. and Kovalenko, S.V. (2002) Tuning rate of the Bergman cyclization of benzannelated enediynes with ortho substituents. Organic Letters, 4(7), 1119-1122.
    • (2002) Organic Letters , vol.4 , Issue.7 , pp. 1119-1122
    • Alabugin, I.V.1    Manoharan, M.2    Kovalenko, S.V.3
  • 241
    • 16444366872 scopus 로고    scopus 로고
    • The effect of charge-transfer complexation/φ-stacking interactions in lowering the activation barrier of the Bergman cyclization
    • Basak, A., Bag, S.S. and Das, A.K. (2005) The effect of charge-transfer complexation/φ-stacking interactions in lowering the activation barrier of the Bergman cyclization. European Journal of Organic Chemistry, (7), 1239-1245.
    • (2005) European Journal of Organic Chemistry , Issue.7 , pp. 1239-1245
    • Basak, A.1    Bag, S.S.2    Das, A.K.3
  • 242
    • 1442311148 scopus 로고    scopus 로고
    • Geometric and electronic control of thermal Bergman cyclization
    • Rawat, D.S. and Zaleski, J.M. (2004) Geometric and electronic control of thermal Bergman cyclization. Synlett, (3), 393-421.
    • (2004) Synlett , Issue.3 , pp. 393-421
    • Rawat, D.S.1    Zaleski, J.M.2
  • 243
    • 32144445389 scopus 로고    scopus 로고
    • Ortho effect in the Bergman cyclization: interception of p-benzyne intermediate by intramolecular hydrogen abstraction
    • Zeidan, T.A., Manoharan, M. and Alabugin, I.V. (2006) Ortho effect in the Bergman cyclization: interception of p-benzyne intermediate by intramolecular hydrogen abstraction. Journal of Organic Chemistry, 71(2), 954-961.
    • (2006) Journal of Organic Chemistry , vol.71 , Issue.2 , pp. 954-961
    • Zeidan, T.A.1    Manoharan, M.2    Alabugin, I.V.3
  • 244
    • 32144446280 scopus 로고    scopus 로고
    • Ortho effect in the Bergman cyclization: comparison of experimental approaches and dissection of cycloaromatization kinetics
    • Zeidan, T.A., Kovalenko, S.V., Manoharan, M. and Alabugin, I.V. (2006) Ortho effect in the Bergman cyclization: comparison of experimental approaches and dissection of cycloaromatization kinetics. Journal of Organic Chemistry, 71(3), 962-975.
    • (2006) Journal of Organic Chemistry , vol.71 , Issue.3 , pp. 962-975
    • Zeidan, T.A.1    Kovalenko, S.V.2    Manoharan, M.3    Alabugin, I.V.4
  • 245
    • 76149095686 scopus 로고    scopus 로고
    • Conformationally gated fragmentations and rearrangements promoted by interception of the Bergman cyclization through intramolecular H-abstraction: a possible mechanism of auto-resistance to natural enediyne antibiotics?
    • Baroudi, A., Mauldin, J. and Alabugin, V.V. (2010) Conformationally gated fragmentations and rearrangements promoted by interception of the Bergman cyclization through intramolecular H-abstraction: a possible mechanism of auto-resistance to natural enediyne antibiotics? Journal of the American Chemical Society, 132(3), 967-979.
    • (2010) Journal of the American Chemical Society , vol.132 , Issue.3 , pp. 967-979
    • Baroudi, A.1    Mauldin, J.2    Alabugin, V.V.3
  • 246
    • 0002791310 scopus 로고    scopus 로고
    • A reiterative approach to 2,3-disubstituted naphthalenes and anthracenes
    • Bowles, D.M. and Anthony, G.E. (2000) A reiterative approach to 2,3-disubstituted naphthalenes and anthracenes. Organic Letters, 2(1), 85-87.
    • (2000) Organic Letters , vol.2 , Issue.1 , pp. 85-87
    • Bowles, D.M.1    Anthony, G.E.2
  • 247
    • 0028149664 scopus 로고
    • Photochemical analogue of the Bergman cycloaromatization reaction
    • Turro, N., Evenzahav, A. and Nicolaou, K.C. (1994) Photochemical analogue of the Bergman cycloaromatization reaction. Tetrahedron Letters, 35(44), 8089-8092.
    • (1994) Tetrahedron Letters , vol.35 , Issue.44 , pp. 8089-8092
    • Turro, N.1    Evenzahav, A.2    Nicolaou, K.C.3
  • 248
    • 79960170039 scopus 로고    scopus 로고
    • Syntheses and reactivity of naphthalenyl-substituted arenediynes
    • Korovina, N.V., Chang, M.L., Nguyen, T.T., et al. (2011) Syntheses and reactivity of naphthalenyl-substituted arenediynes. Organic Letters, 13(14), 3660-3663.
    • (2011) Organic Letters , vol.13 , Issue.14 , pp. 3660-3663
    • Korovina, N.V.1    Chang, M.L.2    Nguyen, T.T.3
  • 249
    • 0141765936 scopus 로고    scopus 로고
    • Highly efficient photochemical generation of a triple bond: synthesis, properties, and photodecarbonylation of cyclopropenones
    • Poloukhtine, A. and Popik, V.V. (2003) Highly efficient photochemical generation of a triple bond: synthesis, properties, and photodecarbonylation of cyclopropenones. Journal of Organic Chemistry, 68(20), 7833-7840.
    • (2003) Journal of Organic Chemistry , vol.68 , Issue.20 , pp. 7833-7840
    • Poloukhtine, A.1    Popik, V.V.2
  • 251
    • 14544268963 scopus 로고    scopus 로고
    • Photoswitchable enediynes: use of cyclopropenone as photocleavable masking group for the enediyne triple bond
    • Poloukhtine, A. and Popik, V.V. (2005) Photoswitchable enediynes: use of cyclopropenone as photocleavable masking group for the enediyne triple bond. Journal of the Chemical Society, Chemical Communications, (5), 617-619.
    • (2005) Journal of the Chemical Society, Chemical Communications , Issue.5 , pp. 617-619
    • Poloukhtine, A.1    Popik, V.V.2
  • 252
    • 33749015722 scopus 로고    scopus 로고
    • Two-photon photochemical generation of reactive enediyne
    • Poloukhtine, A. and Popik, V.V. (2006) Two-photon photochemical generation of reactive enediyne. Journal of Organic Chemistry, 71(19), 7417-7421.
    • (2006) Journal of Organic Chemistry , vol.71 , Issue.19 , pp. 7417-7421
    • Poloukhtine, A.1    Popik, V.V.2
  • 253
    • 51349143055 scopus 로고    scopus 로고
    • Enhancement of the reactivity of photochemically generated enediynes via keto-enol tautomerization
    • Karpov, G.V., Kuzmin, A. and Popik, V.V. (2008) Enhancement of the reactivity of photochemically generated enediynes via keto-enol tautomerization. Journal of the American Chemical Society, 130(35), 11771-11777.
    • (2008) Journal of the American Chemical Society , vol.130 , Issue.35 , pp. 11771-11777
    • Karpov, G.V.1    Kuzmin, A.2    Popik, V.V.3
  • 255
    • 0242666398 scopus 로고    scopus 로고
    • experimental and theoretical investigation of reversible interconversion, thermal reactions, and wavelength-dependent photochemistry of diazo Meldrum's acid and its diazirine isomer, 6,6-dimethyl-5, 7-dioxa-1,2-diaza-spiro[2,5]oct-1-ene-4,8-dione
    • Bogdanova, A. and Popik, V.V. (2003) experimental and theoretical investigation of reversible interconversion, thermal reactions, and wavelength-dependent photochemistry of diazo Meldrum's acid and its diazirine isomer, 6,6-dimethyl-5, 7-dioxa-1,2-diaza-spiro[2,5]oct-1-ene-4,8-dione. Journal of the American Chemical Society, 125(46), 14153-14162.
    • (2003) Journal of the American Chemical Society , vol.125 , Issue.46 , pp. 14153-14162
    • Bogdanova, A.1    Popik, V.V.2
  • 256
    • 62649147508 scopus 로고    scopus 로고
    • Photochemical generation and reversible cycloaromatization of a nine-membered ring cyclic enediyne
    • Pandithavidana, D.R., Poloukhtine, A. and Popik, V.V. (2009) Photochemical generation and reversible cycloaromatization of a nine-membered ring cyclic enediyne. Journal of the American Chemical Society, 131(1), 351-356.
    • (2009) Journal of the American Chemical Society , vol.131 , Issue.1 , pp. 351-356
    • Pandithavidana, D.R.1    Poloukhtine, A.2    Popik, V.V.3
  • 260
    • 0028225955 scopus 로고
    • Synthesis and reactivity of the first bis(crown ether) enediyne
    • Konig, B. and Rutters, H. (1994) Synthesis and reactivity of the first bis(crown ether) enediyne. Tetrahedron Letters, 35(21), 3501-3504.
    • (1994) Tetrahedron Letters , vol.35 , Issue.21 , pp. 3501-3504
    • Konig, B.1    Rutters, H.2
  • 262
    • 0000005509 scopus 로고
    • Organometallic diradical cycloaromatization reaction
    • Wang, Y. and Finn, M.G. (1995) Organometallic diradical cycloaromatization reaction. Journal of the American Chemical Society, 117(30), 8045-8046.
    • (1995) Journal of the American Chemical Society , vol.117 , Issue.30 , pp. 8045-8046
    • Wang, Y.1    Finn, M.G.2
  • 263
    • 0033582580 scopus 로고    scopus 로고
    • W (CO)5 THF-catalyzed electrocyclizations of aromatic enynes via vinylidene intermediates
    • Maeyema, K. and Iwasawa, N. (1999) W (CO)5 THF-catalyzed electrocyclizations of aromatic enynes via vinylidene intermediates. Journal of Organic Chemistry, 64(4), 1344-1346.
    • (1999) Journal of Organic Chemistry , vol.64 , Issue.4 , pp. 1344-1346
    • Maeyema, K.1    Iwasawa, N.2
  • 264
    • 0029860625 scopus 로고    scopus 로고
    • Ruthenium-catalyzed cyclizations of dienylalkynes via vinylidene intermediates
    • Merlic, C.A. and Pauly, M.E. (1996) Ruthenium-catalyzed cyclizations of dienylalkynes via vinylidene intermediates. Journal of the American Chemical Society, 118(45), 11319-11320.
    • (1996) Journal of the American Chemical Society , vol.118 , Issue.45 , pp. 11319-11320
    • Merlic, C.A.1    Pauly, M.E.2
  • 265
  • 266
    • 0000782213 scopus 로고    scopus 로고
    • New examples of 1,6-and 1,7-hydrogen transfer promoted by an α-silyl group in rhodium(I)-catalyzed radical reactions of acyclic enediynes
    • Manabe, T., Yanagi, S.-I., Ohe, K. and Uemura, S. (1998) New examples of 1,6-and 1,7-hydrogen transfer promoted by an α-silyl group in rhodium(I)-catalyzed radical reactions of acyclic enediynes. Organometallics, 17(14), 2942-2944.
    • (1998) Organometallics , vol.17 , Issue.14 , pp. 2942-2944
    • Manabe, T.1    Yanagi, S.-I.2    Ohe, K.3    Uemura, S.4
  • 267
    • 0001457942 scopus 로고
    • Arene 1, 4-diradical formation from o-dialkynylarenes
    • Semmelhack, M.F., Neu, T. and Foubelo, F. (1994) Arene 1, 4-diradical formation from o-dialkynylarenes. Journal of Organic Chemistry, 59(17), 5038-5047.
    • (1994) Journal of Organic Chemistry , vol.59 , Issue.17 , pp. 5038-5047
    • Semmelhack, M.F.1    Neu, T.2    Foubelo, F.3
  • 268
    • 0034614070 scopus 로고    scopus 로고
    • Inhibition and acceleration of the Bergman cycloaromatization reaction by the pentamethylcyclopentadienyl ruthenium cation
    • O'Connor, J.M., Lee, L.I., Gantzel, P. and Lam, K.-C. (2000) Inhibition and acceleration of the Bergman cycloaromatization reaction by the pentamethylcyclopentadienyl ruthenium cation. Journal of the American Chemical Society, 122(48), 12057-12058.
    • (2000) Journal of the American Chemical Society , vol.122 , Issue.48 , pp. 12057-12058
    • O'Connor, J.M.1    Lee, L.I.2    Gantzel, P.3    Lam, K.-C.4
  • 269
    • 77955575940 scopus 로고    scopus 로고
    • A photochemical metallocene route to anionic enediynes: synthesis, solid-state structures, and ab initio computations on cyclopentadienidoenediynes
    • O'Connor, J.M., Baldridge, K.K., Rodgers, B.L., et al. (2010) A photochemical metallocene route to anionic enediynes: synthesis, solid-state structures, and ab initio computations on cyclopentadienidoenediynes. Journal of the American Chemical Society, 132(32), 11030-11032.
    • (2010) Journal of the American Chemical Society , vol.132 , Issue.32 , pp. 11030-11032
    • O'Connor, J.M.1    Baldridge, K.K.2    Rodgers, B.L.3
  • 272
    • 33645021480 scopus 로고    scopus 로고
    • Platinum-catalyzed aromatization of enediynes via a C-H Bond insertion of tethered alkanes
    • Taduri, B.P., Ran, Y.-F., Huang, C.-W. and Liu, R.S. (2006) Platinum-catalyzed aromatization of enediynes via a C-H Bond insertion of tethered alkanes. Organic Letters, 8(5), 883-886.
    • (2006) Organic Letters , vol.8 , Issue.5 , pp. 883-886
    • Taduri, B.P.1    Ran, Y.-F.2    Huang, C.-W.3    Liu, R.S.4
  • 273
    • 26844524327 scopus 로고    scopus 로고
    • Molybdenum-mediated cyclocarbonylation of 1-ethynyl-2-allenylbenzenes to 1H-cyclopenta[a]inden-2-ones
    • Datta, S. and Liu, R.-S. (2005) Molybdenum-mediated cyclocarbonylation of 1-ethynyl-2-allenylbenzenes to 1H-cyclopenta[a]inden-2-ones. Tetrahedron Letters, 46(46), 7985-7988.
    • (2005) Tetrahedron Letters , vol.46 , Issue.46 , pp. 7985-7988
    • Datta, S.1    Liu, R.-S.2
  • 274
    • 33745035640 scopus 로고    scopus 로고
    • Synthesis of aromatic ketones by a transition metal-catalyzed tandem sequence
    • Zhao, J., Hughes, C.O. and Toste, F.D. (2006) Synthesis of aromatic ketones by a transition metal-catalyzed tandem sequence. Journal of the American Chemical Society, 128(23), 7436-7437.
    • (2006) Journal of the American Chemical Society , vol.128 , Issue.23 , pp. 7436-7437
    • Zhao, J.1    Hughes, C.O.2    Toste, F.D.3
  • 276
    • 0024343657 scopus 로고
    • Biradical formation from acyclic conjugated eneyne-allene system related to neocarzinostatin and esperamicin-calichemicin
    • Nagata, R., Yamanaka, H., Okazaki, E. and Saito, I. (1989) Biradical formation from acyclic conjugated eneyne-allene system related to neocarzinostatin and esperamicin-calichemicin. Tetrahedron Letters, 30(37), 4995-4998.
    • (1989) Tetrahedron Letters , vol.30 , Issue.37 , pp. 4995-4998
    • Nagata, R.1    Yamanaka, H.2    Okazaki, E.3    Saito, I.4
  • 277
    • 0025299412 scopus 로고
    • DNA cleavage by acyclic eneyne-allene systems related to neocarzinostatin and esperamicin-calicheamicin
    • Nagata, R., Yamanaka, H., Murahashi, E. and Saito, I. (1990) DNA cleavage by acyclic eneyne-allene systems related to neocarzinostatin and esperamicin-calicheamicin. Tetrahedron Letters, 31(20), 2907-2910.
    • (1990) Tetrahedron Letters , vol.31 , Issue.20 , pp. 2907-2910
    • Nagata, R.1    Yamanaka, H.2    Murahashi, E.3    Saito, I.4
  • 278
    • 0029034833 scopus 로고
    • Switching from the Myers reaction to a new thermal cyclization mode in enyne-allenes
    • Schmittel, M., Strittmatter, M. and Kiau, S. (1995) Switching from the Myers reaction to a new thermal cyclization mode in enyne-allenes. Tetrahedron Letters, 36(28), 4975-4978.
    • (1995) Tetrahedron Letters , vol.36 , Issue.28 , pp. 4975-4978
    • Schmittel, M.1    Strittmatter, M.2    Kiau, S.3
  • 279
    • 20344378706 scopus 로고    scopus 로고
    • 6 cyclization of enyne-allenes: experimental evidence supports a stepwise mechanism
    • 6 cyclization of enyne-allenes: experimental evidence supports a stepwise mechanism. Journal of Organic Chemistry, 70(12), 4865-4868.
    • (2005) Journal of Organic Chemistry , vol.70 , Issue.12 , pp. 4865-4868
    • Schmittel, M.1    Vavilala, C.2
  • 281
    • 0034833555 scopus 로고    scopus 로고
    • The importance of the ene reaction for the C2-C6 cyclization of enyne-allenes
    • Musch, P.W. and Engels, B., (2001) The importance of the ene reaction for the C2-C6 cyclization of enyne-allenes. Journal of the American Chemical Society, 123(23), 5557-5562.
    • (2001) Journal of the American Chemical Society , vol.123 , Issue.23 , pp. 5557-5562
    • Musch, P.W.1    Engels, B.2
  • 284
    • 76749153901 scopus 로고    scopus 로고
    • Intramolecular Diels-Alder reaction in enyne-allenes: a computational investigation and comparison with the Myers-Saito and Schmittel reactions
    • Chen, H.-T., Chen, H.-L. and Ho, J.-J. (2010) Intramolecular Diels-Alder reaction in enyne-allenes: a computational investigation and comparison with the Myers-Saito and Schmittel reactions. Journal of Physical Organic Chemistry, 23(2), 134-140.
    • (2010) Journal of Physical Organic Chemistry , vol.23 , Issue.2 , pp. 134-140
    • Chen, H.-T.1    Chen, H.-L.2    Ho, J.-J.3
  • 285
    • 56549110014 scopus 로고    scopus 로고
    • 6 cyclization of enyne-allenes: detection of a fulvene triplet diradical in the laser flash photolysis
    • 6 cyclization of enyne-allenes: detection of a fulvene triplet diradical in the laser flash photolysis. Journal of Organic Chemistry, 73(22), 8815-8828.
    • (2008) Journal of Organic Chemistry , vol.73 , Issue.22 , pp. 8815-8828
    • Bucher, G.1    Mahajan, A.A.2    Schmittel, M.3
  • 286
    • 0037040670 scopus 로고    scopus 로고
    • Aromaticity of the Bergman, Myers-Saito, Schmittel, and directly related cyclizations of enediynes
    • Stahl, F., Moran, D., von Ragúe Schleyer, P., Prall, M. and Schreiner, P.R. (2002) Aromaticity of the Bergman, Myers-Saito, Schmittel, and directly related cyclizations of enediynes. Journal of Organic Chemistry, 67(5), 1453-1461.
    • (2002) Journal of Organic Chemistry , vol.67 , Issue.5 , pp. 1453-1461
    • Stahl, F.1    Moran, D.2    von Ragúe Schleyer, P.3    Prall, M.4    Schreiner, P.R.5
  • 287
    • 0033595573 scopus 로고    scopus 로고
    • 6 ("Schmittel") cyclizations of parent and monocyclic enyne-allenes: challenges to chemistry and computation
    • 6 ("Schmittel") cyclizations of parent and monocyclic enyne-allenes: challenges to chemistry and computation. Journal of the American Chemical Society, 121(37), 8615-8627.
    • (1999) Journal of the American Chemical Society , vol.121 , Issue.37 , pp. 8615-8627
    • Schreiner, P.R.1    Prall, M.2
  • 289
    • 37649024439 scopus 로고    scopus 로고
    • Synthesis and structures of helical polycyclic aromatic hydrocarbons bearing aryl substituents at the most sterically hindered positions
    • Zhang, Y.Z., Petersen, J.L. and Wang, K.K. (2008) Synthesis and structures of helical polycyclic aromatic hydrocarbons bearing aryl substituents at the most sterically hindered positions. Tetrahedron, 64(7), 1285-1289.
    • (2008) Tetrahedron , vol.64 , Issue.7 , pp. 1285-1289
    • Zhang, Y.Z.1    Petersen, J.L.2    Wang, K.K.3
  • 291
    • 23644457959 scopus 로고    scopus 로고
    • Synthesis of indeno-fused derivatives of quinolizinium salts, imidazo[1,2-a]pyridine, Pyrido[1,2-a]indole, and 4Hquinolizin-4-one via benzannulated enyne-allenes
    • Dai, W., Petersen, J.L. and Wang, K.K. (2005) Synthesis of indeno-fused derivatives of quinolizinium salts, imidazo[1,2-a]pyridine, Pyrido[1,2-a]indole, and 4Hquinolizin-4-one via benzannulated enyne-allenes. Journal of Organic Chemistry, 70(17), 6647-6652.
    • (2005) Journal of Organic Chemistry , vol.70 , Issue.17 , pp. 6647-6652
    • Dai, W.1    Petersen, J.L.2    Wang, K.K.3
  • 292
    • 0035812781 scopus 로고    scopus 로고
    • Biradicals from benzoenyne-allenes. Application in the synthesis of 11H-benzo[b]fluoren-11-ols,1Hcyclobut[ a]indenes, and related compounds
    • Li, H., Zhang, H.-R., Petersen, J.L. and Wang, K.K. (2001 Biradicals from benzoenyne-allenes. Application in the synthesis of 11H-benzo[b]fluoren-11-ols,1Hcyclobut[ a]indenes, and related compounds. Journal of Organic Chemistry, 66(20), 6662-6668.
    • (2001) Journal of Organic Chemistry , vol.66 , Issue.20 , pp. 6662-6668
    • Li, H.1    Zhang, H.-R.2    Petersen, J.L.3    Wang, K.K.4
  • 293
    • 0032721872 scopus 로고    scopus 로고
    • Synthesis of a C44H26 hydrocarbon having a carbon framework represented on the surface of C60 via benzoenyne-allenes
    • Zhang, H.-R. and Wang, K.K. (1999) Synthesis of a C44H26 hydrocarbon having a carbon framework represented on the surface of C60 via benzoenyne-allenes. Journal of Organic Chemistry, 64(21), 7996-7999.
    • (1999) Journal of Organic Chemistry , vol.64 , Issue.21 , pp. 7996-7999
    • Zhang, H.-R.1    Wang, K.K.2
  • 294
    • 0142227963 scopus 로고    scopus 로고
    • Polycyclic aromatic compounds via radical cyclizations of benzannulated enyne-allenes derived from Ireland-Claisen Rearrangement
    • Yang, Y., Petersen, J.L. and Wang, K.K. (2003) Polycyclic aromatic compounds via radical cyclizations of benzannulated enyne-allenes derived from Ireland-Claisen Rearrangement. Journal of Organic Chemistry, 68(22), 8545-8549.
    • (2003) Journal of Organic Chemistry , vol.68 , Issue.22 , pp. 8545-8549
    • Yang, Y.1    Petersen, J.L.2    Wang, K.K.3
  • 295
    • 0001028020 scopus 로고    scopus 로고
    • Tandem enyne allene-radical cyclization: low-temperature approaches to benz[e]indene and indene compounds
    • Grissom, J.W., Klingberg, D., Huang, D. and Slattery, B.J. (1997) Tandem enyne allene-radical cyclization: low-temperature approaches to benz[e]indene and indene compounds. Journal of Organic Chemistry, 62(3), 603-626.
    • (1997) Journal of Organic Chemistry , vol.62 , Issue.3 , pp. 603-626
    • Grissom, J.W.1    Klingberg, D.2    Huang, D.3    Slattery, B.J.4
  • 296
    • 0032783949 scopus 로고    scopus 로고
    • Synthesis of anti-and syn-diol epoxides of trans-3,4-dihydroxy-3,4-dihydrobenzo[ghi]fluoranthene: model planar diol epoxides
    • Chang, H.-F. and Cho, B.P. (1999) Synthesis of anti-and syn-diol epoxides of trans-3,4-dihydroxy-3,4-dihydrobenzo[ghi]fluoranthene: model planar diol epoxides. Journal of Organic Chemistry, 64(25), 9051-9056.
    • (1999) Journal of Organic Chemistry , vol.64 , Issue.25 , pp. 9051-9056
    • Chang, H.-F.1    Cho, B.P.2
  • 298
    • 0037131288 scopus 로고    scopus 로고
    • 1,1',3,3',6,6',8,8'-octachloro-9,9'-bifluorenylidene and perchloro-9, 9'-bifluorenylidene, two exceedingly twisted ethylenes
    • Molins, E., Miravitlles, C. and Ballester, M. (2002) 1,1',3,3',6,6',8,8'-octachloro-9,9'-bifluorenylidene and perchloro-9, 9'-bifluorenylidene, two exceedingly twisted ethylenes. Journal of Organic Chemistry, 67(21), 7175-7178.
    • (2002) Journal of Organic Chemistry , vol.67 , Issue.21 , pp. 7175-7178
    • Molins, E.1    Miravitlles, C.2    Ballester, M.3
  • 300
    • 15444374450 scopus 로고    scopus 로고
    • Synthesis of diindeno-fused 4H-cyclopenta[def]phenanthren-4-ones and related compounds via benzannulated enediynyl propargylic alcohols
    • Han, X.Q., Zhang, Y.Z. and Wang, K.K. (2005) Synthesis of diindeno-fused 4H-cyclopenta[def]phenanthren-4-ones and related compounds via benzannulated enediynyl propargylic alcohols. Journal of Organic Chemistry, 70(6), 2406-2408.
    • (2005) Journal of Organic Chemistry , vol.70 , Issue.6 , pp. 2406-2408
    • Han, X.Q.1    Zhang, Y.Z.2    Wang, K.K.3
  • 301
    • 14744273171 scopus 로고    scopus 로고
    • Structure-property relationships of donor/acceptor-functionalized tetrakis (phenylethynyl)benzenes and bis(dehydrobenzoannuleno)benzenes
    • Marsden, J.A., Miller, J.J., Shirtcliff, L.D. and Haley, M.M. (2005) Structure-property relationships of donor/acceptor-functionalized tetrakis (phenylethynyl)benzenes and bis(dehydrobenzoannuleno)benzenes. Journal of the American Chemical Society, 127(8), 2464-2476.
    • (2005) Journal of the American Chemical Society , vol.127 , Issue.8 , pp. 2464-2476
    • Marsden, J.A.1    Miller, J.J.2    Shirtcliff, L.D.3    Haley, M.M.4
  • 302
    • 14544268554 scopus 로고    scopus 로고
    • Generation and characterization of highly strained dibenzotetrakisdehydro[12] and dibenzopentakisdehydro[14] annulenes
    • Hisaki, I., Eda, T., Sonoda, M., et al. (2005) Generation and characterization of highly strained dibenzotetrakisdehydro[12] and dibenzopentakisdehydro[14] annulenes. Journal of Organic Chemistry, 70(5), 1853-1864.
    • (2005) Journal of Organic Chemistry , vol.70 , Issue.5 , pp. 1853-1864
    • Hisaki, I.1    Eda, T.2    Sonoda, M.3
  • 303
    • 33645125970 scopus 로고    scopus 로고
    • Synthesis and inclusion properties of 6,6'-bi(benzo[b]fluoren-5-ol) derivative by cycloaromatization
    • Kawano, T., Suehiro, M. and Ueda, I. (2006) Synthesis and inclusion properties of 6,6'-bi(benzo[b]fluoren-5-ol) derivative by cycloaromatization. Chemistry Letters, 35(1), 58-59.
    • (2006) Chemistry Letters , vol.35 , Issue.1 , pp. 58-59
    • Kawano, T.1    Suehiro, M.2    Ueda, I.3
  • 304
    • 36849043614 scopus 로고    scopus 로고
    • Construction of unusual and congested polycyclic structures via benzannulated enediynyl alcohols derived from truxenone
    • Wang, Y.-H., Akhmedov, N.G., Petersen, J.L. and Wang, K.K. (2007) Construction of unusual and congested polycyclic structures via benzannulated enediynyl alcohols derived from truxenone. Journal of Organic Chemistry, 72(25), 9604-9608.
    • (2007) Journal of Organic Chemistry , vol.72 , Issue.25 , pp. 9604-9608
    • Wang, Y.-H.1    Akhmedov, N.G.2    Petersen, J.L.3    Wang, K.K.4
  • 305
    • 9444256311 scopus 로고    scopus 로고
    • Synthesis and structure of a helical diindenophenanthrene with four congested phenyl substituents as a molecular spiral staircase
    • Dai, W., Petersen, J.L. and Wang, K.K. (2004) Synthesis and structure of a helical diindenophenanthrene with four congested phenyl substituents as a molecular spiral staircase. Organic Letters, 6(23), 4355-4357.
    • (2004) Organic Letters , vol.6 , Issue.23 , pp. 4355-4357
    • Dai, W.1    Petersen, J.L.2    Wang, K.K.3
  • 306
    • 33947581990 scopus 로고    scopus 로고
    • Synthesis and structures of diindeno-fused 1,12-diphenylbenzo[c]phenanthrene and 1,14-diphenyl[5]helicene bearing severe helical twists
    • Zhang, Y., Petersen, J.L. and Wang, K.K. (2007) Synthesis and structures of diindeno-fused 1,12-diphenylbenzo[c]phenanthrene and 1,14-diphenyl[5]helicene bearing severe helical twists. Organic Letters, 9(6), 1025-1028.
    • (2007) Organic Letters , vol.9 , Issue.6 , pp. 1025-1028
    • Zhang, Y.1    Petersen, J.L.2    Wang, K.K.3
  • 307
    • 33646082273 scopus 로고    scopus 로고
    • Ring expansion of 11H-benzo[b]fluorene-11-methanols and related compounds leading to17,18-diphenyldibenzo[a,o]pentaphene and related polycyclic aromatic hydrocarbons with extended conjugation and novel architectures
    • Yang, Y., Dai, W., Zhang, Y., Petersen, J.L. and Wang, K.K. (2006) Ring expansion of 11H-benzo[b]fluorene-11-methanols and related compounds leading to17,18-diphenyldibenzo[a,o]pentaphene and related polycyclic aromatic hydrocarbons with extended conjugation and novel architectures. Tetrahedron, 62(18), 4364-4371.
    • (2006) Tetrahedron , vol.62 , Issue.18 , pp. 4364-4371
    • Yang, Y.1    Dai, W.2    Zhang, Y.3    Petersen, J.L.4    Wang, K.K.5
  • 308
    • 33745685085 scopus 로고    scopus 로고
    • Synthesis and separation of the atropisomers of 2-(5-benzo[b]fluorenyl)-2'-hydroxy-1,1'-binaphthyl and related compounds
    • Yang, H., Petersen, J.L. and Wang, K.K. (2006) Synthesis and separation of the atropisomers of 2-(5-benzo[b]fluorenyl)-2'-hydroxy-1,1'-binaphthyl and related compounds. Tetrahedron, 62(34), 8133-8141.
    • (2006) Tetrahedron , vol.62 , Issue.34 , pp. 8133-8141
    • Yang, H.1    Petersen, J.L.2    Wang, K.K.3
  • 309
    • 29744441903 scopus 로고    scopus 로고
    • Synthesis and rotational barriers of atropisomers of 1,2-bis[5-(11H-benzo[b]fluorenyl)]benzenes and related compounds
    • Yang, H., Petersen, J.L. and Wang, K.K. (2006) Synthesis and rotational barriers of atropisomers of 1,2-bis[5-(11H-benzo[b]fluorenyl)]benzenes and related compounds. Tetrahedron, 62(6), 1231-1238.
    • (2006) Tetrahedron , vol.62 , Issue.6 , pp. 1231-1238
    • Yang, H.1    Petersen, J.L.2    Wang, K.K.3
  • 310
    • 0038537375 scopus 로고    scopus 로고
    • Molecules with helical structure: how to build a molecular spiral staircase
    • Schmuck, C. (2003) Molecules with helical structure: how to build a molecular spiral staircase. Angewandte Chemie International Edition, 42(22), 2448-2452.
    • (2003) Angewandte Chemie International Edition , vol.42 , Issue.22 , pp. 2448-2452
    • Schmuck, C.1
  • 311
    • 0141676773 scopus 로고    scopus 로고
    • Recent developments in the synthesis of helicene-like molecules
    • Urbano, A. (2003) Recent developments in the synthesis of helicene-like molecules. Angewandte Chemie International Edition, 42(34), 3986-3989.
    • (2003) Angewandte Chemie International Edition , vol.42 , Issue.34 , pp. 3986-3989
    • Urbano, A.1
  • 312
    • 0142196838 scopus 로고    scopus 로고
    • Functionalizations of [6]-and [7]helicenes at their most sterically hindered positions
    • Paruch, K., Vyklický, L., Wang, D.Z., et al. (2003) Functionalizations of [6]-and [7]helicenes at their most sterically hindered positions. Journal of Organic Chemistry, 68(22), 8539-8544.
    • (2003) Journal of Organic Chemistry , vol.68 , Issue.22 , pp. 8539-8544
    • Paruch, K.1    Vyklický, L.2    Wang, D.Z.3
  • 313
    • 33745725815 scopus 로고    scopus 로고
    • Synthesis of bowl-shaped polycyclic aromatic hydrocarbons via palladium-catalyzed intramolecular arylation reactions
    • Kim, D., Petersen, J.L. and Wang, K.K. (2006) Synthesis of bowl-shaped polycyclic aromatic hydrocarbons via palladium-catalyzed intramolecular arylation reactions. Organic Letters, 8(11), 2313-2316.
    • (2006) Organic Letters , vol.8 , Issue.11 , pp. 2313-2316
    • Kim, D.1    Petersen, J.L.2    Wang, K.K.3
  • 314
    • 79955065056 scopus 로고    scopus 로고
    • Synthesis of 5-(2-methoxy-1-naphthyl)-and 5-[2-(methoxymethyl)-1-naphthyl]-11Hbenzo[ b]fluorene as 2,2'-disubstituted 1,1'-binaphthyls via benzannulated enyne-allenes
    • Wang, Y.-H., Bailey, J.F., Petersen, J.L. and Wang, K.K. (2011) Synthesis of 5-(2-methoxy-1-naphthyl)-and 5-[2-(methoxymethyl)-1-naphthyl]-11Hbenzo[ b]fluorene as 2,2'-disubstituted 1,1'-binaphthyls via benzannulated enyne-allenes. Beilstein Journal of Organic Chemistry, 7, 496-502.
    • (2011) Beilstein Journal of Organic Chemistry , vol.7 , pp. 496-502
    • Wang, Y.-H.1    Bailey, J.F.2    Petersen, J.L.3    Wang, K.K.4
  • 315
    • 79954618652 scopus 로고    scopus 로고
    • An efficient and recyclable hybrid nanocatalyst to promote enantioselective radical cascade rearrangements of enediynes
    • Nechab, M., Besson, E., Campolo, D., et al. (2011) An efficient and recyclable hybrid nanocatalyst to promote enantioselective radical cascade rearrangements of enediynes. Journal of the Chemical Society, Chemical Communications, (47), 5286-5288.
    • (2011) Journal of the Chemical Society, Chemical Communications , Issue.47 , pp. 5286-5288
    • Nechab, M.1    Besson, E.2    Campolo, D.3
  • 317
    • 0037448899 scopus 로고    scopus 로고
    • Radical-anionic cyclizations of enediynes: remarkable effects of benzannelation and remote substituents on cyclorearomatization reactions
    • Alabugin, I.V. and Manoharan, M. (2003) Radical-anionic cyclizations of enediynes: remarkable effects of benzannelation and remote substituents on cyclorearomatization reactions. Journal of the American Chemical Society, 125(15), 4495-4509.
    • (2003) Journal of the American Chemical Society , vol.125 , Issue.15 , pp. 4495-4509
    • Alabugin, I.V.1    Manoharan, M.2
  • 318
    • 0346970756 scopus 로고    scopus 로고
    • Radical-induced cycloaromatization: routes to fluoranthenes and acephenanthrylenes
    • Scott, J.L., Parkin, S.R. and Anthony, J.E. (2004) Radical-induced cycloaromatization: routes to fluoranthenes and acephenanthrylenes. Synlett, (1), 161-164.
    • (2004) Synlett , Issue.1 , pp. 161-164
    • Scott, J.L.1    Parkin, S.R.2    Anthony, J.E.3
  • 319
    • 0347504845 scopus 로고    scopus 로고
    • Fulvenes from enediynes: regioselective electrophilic domino and tandem cyclizations of enynes and oligoynes
    • Schreiner, P.R., Prall, M. and Lutz, V. (2003) Fulvenes from enediynes: regioselective electrophilic domino and tandem cyclizations of enynes and oligoynes. Angewandte Chemie International Edition, 42(46), 5757-5760.
    • (2003) Angewandte Chemie International Edition , vol.42 , Issue.46 , pp. 5757-5760
    • Schreiner, P.R.1    Prall, M.2    Lutz, V.3
  • 320
    • 0037657968 scopus 로고    scopus 로고
    • Reactant destabilization in the Bergman cyclization and rational design of light-and pH-activated enediynes
    • Alabugin, I.V. and Manoharan, M. (2003) Reactant destabilization in the Bergman cyclization and rational design of light-and pH-activated enediynes. Journal Physical Chemistry A, 107(18), 3363-3371.
    • (2003) Journal Physical Chemistry A , vol.107 , Issue.18 , pp. 3363-3371
    • Alabugin, I.V.1    Manoharan, M.2
  • 321
    • 3242732426 scopus 로고    scopus 로고
    • 5-Exo-dig radical cyclization of enediynes: the first synthesis of tin-substituted benzofulvenes
    • Kovalenko, S.V., Peabody, S., Manoharan, M., Clark, R.J. and Alabugin, I.V. (2004) 5-Exo-dig radical cyclization of enediynes: the first synthesis of tin-substituted benzofulvenes. Organic Letters, 6(14), 2457-2460.
    • (2004) Organic Letters , vol.6 , Issue.14 , pp. 2457-2460
    • Kovalenko, S.V.1    Peabody, S.2    Manoharan, M.3    Clark, R.J.4    Alabugin, I.V.5
  • 325
    • 0042208364 scopus 로고    scopus 로고
    • Control of kinetics and thermodynamics of [1,5]-shifts by aromaticity: a view through the prism of Marcus theory
    • Alabugin, I.V., Manoharan, M., Breiner, B. and Lewis, F.D. (2003) Control of kinetics and thermodynamics of [1,5]-shifts by aromaticity: a view through the prism of Marcus theory. Journal of the American Chemical Society, 125(31), 9329-9342.
    • (2003) Journal of the American Chemical Society , vol.125 , Issue.31 , pp. 9329-9342
    • Alabugin, I.V.1    Manoharan, M.2    Breiner, B.3    Lewis, F.D.4
  • 326
    • 0000655212 scopus 로고    scopus 로고
    • Cyclization of enediyne radical cation through chemical, photochemical, and electrochemical oxidation: the role of state symmetry
    • Ramkumar, D., Kalpana, M., Varghese, B., Sankararaman,S., Jagadeesh, M.N. and Chandrasekhar, J. (1996) Cyclization of enediyne radical cation through chemical, photochemical, and electrochemical oxidation: the role of state symmetry. Journal of Organic Chemistry, 61(6), 2247-2250.
    • (1996) Journal of Organic Chemistry , vol.61 , Issue.6 , pp. 2247-2250
    • Ramkumar, D.1    Kalpana, M.2    Varghese, B.3    Sankararaman, S.4    Jagadeesh, M.N.5    Chandrasekhar, J.6
  • 328
    • 0036736762 scopus 로고    scopus 로고
    • 2-Arylindene metallocenes: conformationally dynamic catalysts to control the structure and properties of polypropylenes
    • Lin, S. and Waymouth, R.M. (2002) 2-Arylindene metallocenes: conformationally dynamic catalysts to control the structure and properties of polypropylenes. Accounts of Chemical Research, 35(9), 765-773.
    • (2002) Accounts of Chemical Research , vol.35 , Issue.9 , pp. 765-773
    • Lin, S.1    Waymouth, R.M.2
  • 329
    • 0035831184 scopus 로고    scopus 로고
    • Carbonyl-and carboxyl-substituted enediynes: synthesis, computations, and thermal reactivity
    • Konig, B., Pitsch, W., Klein, M., Vasold, R., Prall, M. and Schreiner, P.R. (2001) Carbonyl-and carboxyl-substituted enediynes: synthesis, computations, and thermal reactivity. Journal of Organic Chemistry, 66(5), 1742-1746.
    • (2001) Journal of Organic Chemistry , vol.66 , Issue.5 , pp. 1742-1746
    • Konig, B.1    Pitsch, W.2    Klein, M.3    Vasold, R.4    Prall, M.5    Schreiner, P.R.6
  • 330
    • 0030820322 scopus 로고    scopus 로고
    • Synthesis of terminal-biradical compounds consisting of two N-oxyl groups connected with conjugated φ-systems
    • Torii, S., Hase, T., Kuroboshi, M., et al. (1997) Synthesis of terminal-biradical compounds consisting of two N-oxyl groups connected with conjugated φ-systems. Tetrahedron Letters, 38(42), 7391-7394.
    • (1997) Tetrahedron Letters , vol.38 , Issue.42 , pp. 7391-7394
    • Torii, S.1    Hase, T.2    Kuroboshi, M.3
  • 331
    • 50449103168 scopus 로고    scopus 로고
    • Radical cascade transformations of tris(o-aryleneethynylenes) into substituted benzo[α]indeno[2,1-c]fluorenes
    • Alabugin, I.V., Gilmore, K., Patil, S., et al. (2008) Radical cascade transformations of tris(o-aryleneethynylenes) into substituted benzo[α]indeno[2,1-c]fluorenes. Journal of the American Chemical Society, 130(34), 11535-11545.
    • (2008) Journal of the American Chemical Society , vol.130 , Issue.34 , pp. 11535-11545
    • Alabugin, I.V.1    Gilmore, K.2    Patil, S.3
  • 332
    • 84862222135 scopus 로고    scopus 로고
    • Polyaromatic ribbons from oligo-alkynes via selective radical cascade: stitching aromatic rings with polyacetylene bridges
    • Byers, P.M. and Alabugin, I.V. (2012) Polyaromatic ribbons from oligo-alkynes via selective radical cascade: stitching aromatic rings with polyacetylene bridges. Journal of the American Chemical Society, 134(23), 9609-9614.
    • (2012) Journal of the American Chemical Society , vol.134 , Issue.23 , pp. 9609-9614
    • Byers, P.M.1    Alabugin, I.V.2
  • 333
    • 3643118570 scopus 로고
    • Double cycloaromatization of (Z,Z)-deca-3,7-diene-1,5,9-triyne: evidence for the intermediacy and diradical character of 2,6-didehydronaphthalene
    • Bharucha, K.N., Marsh, R.M., Minto, R.E. and Bergman, R.G. (1992) Double cycloaromatization of (Z,Z)-deca-3,7-diene-1,5,9-triyne: evidence for the intermediacy and diradical character of 2,6-didehydronaphthalene. Journal of the American Chemical Society, 114(8), 3120-3121.
    • (1992) Journal of the American Chemical Society , vol.114 , Issue.8 , pp. 3120-3121
    • Bharucha, K.N.1    Marsh, R.M.2    Minto, R.E.3    Bergman, R.G.4
  • 334
    • 0010233146 scopus 로고    scopus 로고
    • From phenylenes to acenes: flash vacuum pyrolytic isomerization of angular[3]phenylene to benzo[ghi]fluoranthene
    • Matzger, A.J. and Vollhardt, K.P.C. (1997) From phenylenes to acenes: flash vacuum pyrolytic isomerization of angular[3]phenylene to benzo[ghi]fluoranthene. Journal of the Chemical Society, Chemical Communications, (15), 1415-1416.
    • (1997) Journal of the Chemical Society, Chemical Communications , Issue.15 , pp. 1415-1416
    • Matzger, A.J.1    Vollhardt, K.P.C.2
  • 335
    • 0030824780 scopus 로고    scopus 로고
    • Synthesis, double cycloaromatization, and DNAcleaving activities of (Z,Z)-11-sulfonylundeca-3,7-diene-1,5,9-triyne system
    • Lin, C.-F. and Wu, M.-J. (1997) Synthesis, double cycloaromatization, and DNAcleaving activities of (Z,Z)-11-sulfonylundeca-3,7-diene-1,5,9-triyne system. Journal of Organic Chemistry, 62(13), 4546-4548.
    • (1997) Journal of Organic Chemistry , vol.62 , Issue.13 , pp. 4546-4548
    • Lin, C.-F.1    Wu, M.-J.2
  • 336
    • 24744453294 scopus 로고    scopus 로고
    • Thermodynamic and strain effects in the competition between 5-exo-dig and 6-endo-dig cyclizations of vinyl and aryl radicals
    • Alabugin, I.V. and Manoharan, M. (2005) Thermodynamic and strain effects in the competition between 5-exo-dig and 6-endo-dig cyclizations of vinyl and aryl radicals. Journal of the American Chemical Society, 127(36), 12583-12594.
    • (2005) Journal of the American Chemical Society , vol.127 , Issue.36 , pp. 12583-12594
    • Alabugin, I.V.1    Manoharan, M.2
  • 337
    • 0000228332 scopus 로고
    • Lithium-induced cyclization of tribenzocyclotriynes
    • Youngs, W.J., Djebli, A. and Tessier, C.A. (1991) Lithium-induced cyclization of tribenzocyclotriynes. Organometallics, 10(7), 2089-2090.
    • (1991) Organometallics , vol.10 , Issue.7 , pp. 2089-2090
    • Youngs, W.J.1    Djebli, A.2    Tessier, C.A.3
  • 338
    • 33646029430 scopus 로고    scopus 로고
    • Reductive Bergman-type cyclizations of cross-conjugated enediynes to fulvene and fulvalene anions: the role of the substituent
    • Treitel, N., Eshdat, L., Sheradsky, T., et al. (2006) Reductive Bergman-type cyclizations of cross-conjugated enediynes to fulvene and fulvalene anions: the role of the substituent. Journal of the American Chemical Society, 128(14), 4703-4709.
    • (2006) Journal of the American Chemical Society , vol.128 , Issue.14 , pp. 4703-4709
    • Treitel, N.1    Eshdat, L.2    Sheradsky, T.3
  • 340
    • 4644225203 scopus 로고    scopus 로고
    • Cyclization reactions of dianions in organic synthesis
    • Langer, P. and Freiberg, W. (2004) Cyclization reactions of dianions in organic synthesis. Chemical Review, 104(9), 4125-4150.
    • (2004) Chemical Review , vol.104 , Issue.9 , pp. 4125-4150
    • Langer, P.1    Freiberg, W.2
  • 341
    • 0037162771 scopus 로고    scopus 로고
    • Anionic cycloaromatization of 1-aryl-3-hexen-1,5-diynes initiated by methoxide addition: synthesis of phenanthridinones, benzo[c]phenanthridinones, and biaryls
    • Wu, M.-J., Lin, C.-F. and Lu, W.-D. (2002) Anionic cycloaromatization of 1-aryl-3-hexen-1,5-diynes initiated by methoxide addition: synthesis of phenanthridinones, benzo[c]phenanthridinones, and biaryls. Journal of Organic Chemistry, 67(17), 5907-5912.
    • (2002) Journal of Organic Chemistry , vol.67 , Issue.17 , pp. 5907-5912
    • Wu, M.-J.1    Lin, C.-F.2    Lu, W.-D.3
  • 342
    • 0037067062 scopus 로고    scopus 로고
    • A new rutheniumcatalyzed hydrogen-transfer reaction: transformation of 3-benzyl but-1-ynyl ethers into 1,3-dienes and enzaldehyde
    • Yeh, K.-L, Liu, B., Lo, C.-Y., Huang, H.L. and Liu, R.S. (2002) A new rutheniumcatalyzed hydrogen-transfer reaction: transformation of 3-benzyl but-1-ynyl ethers into 1,3-dienes and enzaldehyde. Journal of the American Chemical Society, 124(23), 6510-6511.
    • (2002) Journal of the American Chemical Society , vol.124 , Issue.23 , pp. 6510-6511
    • Yeh K.-L Liu, B.1    Lo, C.-Y.2    Huang, H.L.3    Liu, R.S.4
  • 343
    • 13844271408 scopus 로고    scopus 로고
    • Reaction of (Z)-1-aryl-3-hexen-1,5-diynes with sodium azide: synthesis of 1-aryl-1H-benzotriazoles
    • Chen, Z.Y. and Wu, M.J. (2005) Reaction of (Z)-1-aryl-3-hexen-1,5-diynes with sodium azide: synthesis of 1-aryl-1H-benzotriazoles. Organic Letters, 7(3), 475-477.
    • (2005) Organic Letters , vol.7 , Issue.3 , pp. 475-477
    • Chen, Z.Y.1    Wu, M.J.2
  • 344
    • 0037021087 scopus 로고    scopus 로고
    • A route to 5-substituted dibenzofurans by anionic cycloaromatization of 2-(6-substituted -3-hexen-1,5-diynyl)phenyl tert-butyldimethyl ethers and related molecules
    • Wu, M.J., Lee, C.Y. and Lin, Ch.-F. (2002) A route to 5-substituted dibenzofurans by anionic cycloaromatization of 2-(6-substituted -3-hexen-1,5-diynyl)phenyl tert-butyldimethyl ethers and related molecules. Angewandte Chemie International Edition, 41(21), 4077-4079.
    • (2002) Angewandte Chemie International Edition , vol.41 , Issue.21 , pp. 4077-4079
    • Wu, M.J.1    Lee, C.Y.2    Lin, C.-F.3
  • 345
    • 1642400679 scopus 로고    scopus 로고
    • Synthesis of carbazoles via an intramolecular cyclization of 2-(6-substituted 3(Z)-hexen-1,5-diynyl)anilines and their related molecules
    • Lee, C.Y., Lin, C.-F., Lee, J.L., Chiu, C.C., Lu, W.D. and Wu, M.J. (2004) Synthesis of carbazoles via an intramolecular cyclization of 2-(6-substituted 3(Z)-hexen-1,5-diynyl)anilines and their related molecules. Journal of Organic Chemistry, 69(6), 2106-2110.
    • (2004) Journal of Organic Chemistry , vol.69 , Issue.6 , pp. 2106-2110
    • Lee, C.Y.1    Lin, C.-F.2    Lee, J.L.3    Chiu, C.C.4    Lu, W.D.5    Wu, M.J.6
  • 346
    • 78650333745 scopus 로고    scopus 로고
    • Synthetic development and mechanistic study on Pd(II)-catalyzed cyclization of enediynes to benzo[a]carbazoles
    • Chen, C.-C., Chin, L.-Y., Yang, S.-C. and Wu, M.-J. (2010) Synthetic development and mechanistic study on Pd(II)-catalyzed cyclization of enediynes to benzo[a]carbazoles. Organic Letters, 12(24), 5652-5655.
    • (2010) Organic Letters , vol.12 , Issue.24 , pp. 5652-5655
    • Chen, C.-C.1    Chin, L.-Y.2    Yang, S.-C.3    Wu, M.-J.4
  • 348
    • 42049112993 scopus 로고    scopus 로고
    • Catalytic transformations of terminal alkynes by cationic tris(1-pyrazolyl) borate ruthenium catalysts: versatile chemistry via catalytic allenylidene, vinylidene, and φ-alkyne intermediates
    • Liu, R.-S. (2008) Catalytic transformations of terminal alkynes by cationic tris(1-pyrazolyl) borate ruthenium catalysts: versatile chemistry via catalytic allenylidene, vinylidene, and φ-alkyne intermediates. Synlett, (6), 801-812.
    • (2008) Synlett , Issue.6 , pp. 801-812
    • Liu, R.-S.1
  • 349
    • 34247513435 scopus 로고    scopus 로고
    • Nucleophilic addition to a p-benzyne derived from an enediyne: a new mechanism for halide incorporation into biomolecules
    • Perrin, C.L., Rodgers, B.L. and O'Connor, J.M. (2007) Nucleophilic addition to a p-benzyne derived from an enediyne: a new mechanism for halide incorporation into biomolecules. Journal of the American Chemical Society, 129(15), 4795-4799.
    • (2007) Journal of the American Chemical Society , vol.129 , Issue.15 , pp. 4795-4799
    • Perrin, C.L.1    Rodgers, B.L.2    O'Connor, J.M.3
  • 351
    • 84863266413 scopus 로고    scopus 로고
    • Ambient Schmittel cyclization promoted by chemoselective triazole-gold catalyst
    • Wang, Q., Aparaj, S., Akhmedov, N.G., Petersen, J.L. and Shi, X. (2012) Ambient Schmittel cyclization promoted by chemoselective triazole-gold catalyst. Organic Letters, 14(5), 1334-1337.
    • (2012) Organic Letters , vol.14 , Issue.5 , pp. 1334-1337
    • Wang, Q.1    Aparaj, S.2    Akhmedov, N.G.3    Petersen, J.L.4    Shi, X.5
  • 352
    • 70549092186 scopus 로고    scopus 로고
    • A novel tandem cyclization of condensed 2,3-dialkynylpyrazines into [1,2,3]triazolo[1',5';1,2]pyrido[3,4-b]pyrazines promoted by sodium azide
    • Gulevskaya, A.V., Dang, S.V., Tyaglivy, A.S., et al. (2010) A novel tandem cyclization of condensed 2,3-dialkynylpyrazines into [1,2,3]triazolo[1',5';1,2]pyrido[3,4-b]pyrazines promoted by sodium azide. Tetrahedron, 66(1), 146-151.
    • (2010) Tetrahedron , vol.66 , Issue.1 , pp. 146-151
    • Gulevskaya, A.V.1    Dang, S.V.2    Tyaglivy, A.S.3
  • 354
    • 84860455166 scopus 로고    scopus 로고
    • Reactivity of bispropargyl sulfones under basic conditions: interplay between garratt-braverman and schmittel/myers-saito cyclization pathway
    • Mukherjee, R., Mondal, S. and Basak, A. et al. (2012) Reactivity of bispropargyl sulfones under basic conditions: interplay between garratt-braverman and schmittel/myers-saito cyclization pathway. Chemistry an Asian Journal, 7(5), 957-965.
    • (2012) Chemistry an Asian Journal , vol.7 , Issue.5 , pp. 957-965
    • Mukherjee, R.1    Mondal, S.2    Basak, A.3
  • 355
    • 65349111407 scopus 로고    scopus 로고
    • Design and synthesis of bisenediyne bissulfones and their reactivity under basic condition
    • Das, S. and Basak, A. (2009) Design and synthesis of bisenediyne bissulfones and their reactivity under basic condition. Bioorganic & Medicinal Chemistry Letters, 19(10), 2815-2818.
    • (2009) Bioorganic & Medicinal Chemistry Letters , vol.19 , Issue.10 , pp. 2815-2818
    • Das, S.1    Basak, A.2
  • 356
    • 0030066058 scopus 로고    scopus 로고
    • Cycloaromatization of enediyne model compounds via a reaction cascade triggered by hydrolysis of the β-alkynylmalonates
    • Shibuya, M., Wakyama, M., Naoe, Y., et al. (1996) Cycloaromatization of enediyne model compounds via a reaction cascade triggered by hydrolysis of the β-alkynylmalonates. Tetrahedron Letters, 37(6), 865-868.
    • (1996) Tetrahedron Letters , vol.37 , Issue.6 , pp. 865-868
    • Shibuya, M.1    Wakyama, M.2    Naoe, Y.3
  • 357
    • 0032537209 scopus 로고    scopus 로고
    • pH dependent cycloaromatization of enediyne model compounds via γ-oxo ketene intermediates
    • Suzuki, I., Naoe, Y., Bando, M., Nemoto, H. and Shibuya, M. (1998) pH dependent cycloaromatization of enediyne model compounds via γ-oxo ketene intermediates. Tetrahedron Letters, 39(16), 2361-2364.
    • (1998) Tetrahedron Letters , vol.39 , Issue.16 , pp. 2361-2364
    • Suzuki, I.1    Naoe, Y.2    Bando, M.3    Nemoto, H.4    Shibuya, M.5
  • 358
    • 0034676690 scopus 로고    scopus 로고
    • Synthesis of enediyne model compounds producing toluene diradicals possessing a highly radical character via enyne-allene intermediates
    • Suzuki, I., Wakayama, M., Shigenaga, A., Nemoto, H. and Shibuya, M. (2000) Synthesis of enediyne model compounds producing toluene diradicals possessing a highly radical character via enyne-allene intermediates. Tetrahedron Letters, 41(51), 10019-10023.
    • (2000) Tetrahedron Letters , vol.41 , Issue.51 , pp. 10019-10023
    • Suzuki, I.1    Wakayama, M.2    Shigenaga, A.3    Nemoto, H.4    Shibuya, M.5
  • 359
    • 0030598009 scopus 로고    scopus 로고
    • Pyridoxal-mediated cycloaromatization of an enediyne model system
    • Wakyama, M., Remoto, H. and Shibuya, M. (1996) Pyridoxal-mediated cycloaromatization of an enediyne model system. Tetrahedron Letters, 37(30), 5397-5400.
    • (1996) Tetrahedron Letters , vol.37 , Issue.30 , pp. 5397-5400
    • Wakyama, M.1    Remoto, H.2    Shibuya, M.3
  • 360
    • 84876517807 scopus 로고    scopus 로고
    • How to lose a bond in two ways-the diradical/zwitterion dichotomy in cycloaromatization reactions
    • Peterson, P.W., Mohamed, R.K. and Alabugin, I.V. (2013) How to lose a bond in two ways-the diradical/zwitterion dichotomy in cycloaromatization reactions. European Journal of Organic Chemistry, (13), 2505-2527.
    • (2013) European Journal of Organic Chemistry , Issue.13 , pp. 2505-2527
    • Peterson, P.W.1    Mohamed, R.K.2    Alabugin, I.V.3
  • 362
    • 1642278107 scopus 로고    scopus 로고
    • Convergent approach to the maduropeptin chromophore: aryl ether formation of (R)-3-aryl-3-hydroxypropanamide and cyclization of macrolactam
    • Kato, N., Shimamura, S., Khan, S., Takeda, F., Kikai, Y. and Hirama, M. (2004) Convergent approach to the maduropeptin chromophore: aryl ether formation of (R)-3-aryl-3-hydroxypropanamide and cyclization of macrolactam. Tetrahedron, 60(14), 3161-3172.
    • (2004) Tetrahedron , vol.60 , Issue.14 , pp. 3161-3172
    • Kato, N.1    Shimamura, S.2    Khan, S.3    Takeda, F.4    Kikai, Y.5    Hirama, M.6
  • 363
    • 0037148015 scopus 로고    scopus 로고
    • Evaluation of alkene isomerization as a trigger for enediyne activation
    • Semmelhack, M.F., Sarpong, R., Bergman, J. and Ho, D.M. (2002) Evaluation of alkene isomerization as a trigger for enediyne activation. Tetrahedron Letters, 43(4), 541-544.
    • (2002) Tetrahedron Letters , vol.43 , Issue.4 , pp. 541-544
    • Semmelhack, M.F.1    Sarpong, R.2    Bergman, J.3    Ho, D.M.4
  • 364
    • 0035249348 scopus 로고    scopus 로고
    • Acid-catalyzed cycloaromatization of enediyne model compounds via enyne-allene intermediates
    • Suzuki, I., Shigenaga, A., Nemoto, H. and Shibuya, M. (2001) Acid-catalyzed cycloaromatization of enediyne model compounds via enyne-allene intermediates. Heterocycles, 54(2), 571-576.
    • (2001) Heterocycles , vol.54 , Issue.2 , pp. 571-576
    • Suzuki, I.1    Shigenaga, A.2    Nemoto, H.3    Shibuya, M.4
  • 365
    • 0344334037 scopus 로고    scopus 로고
    • Synthesis and DNA cleavage study of a 10-membered ring enediyne formed via allylic rearrangement
    • Dai, W.-M., Fong, K.C., Lau, C.W., Zhou, L., Hamaguchi, W. and Nishimoto, S. (1999) Synthesis and DNA cleavage study of a 10-membered ring enediyne formed via allylic rearrangement. Journal of Organic Chemistry, 64(3), 682-683.
    • (1999) Journal of Organic Chemistry , vol.64 , Issue.3 , pp. 682-683
    • Dai, W.-M.1    Fong, K.C.2    Lau, C.W.3    Zhou, L.4    Hamaguchi, W.5    Nishimoto, S.6
  • 366
    • 0035908216 scopus 로고    scopus 로고
    • Neighboring nucleophilic group assisted rearrangement of allylic esters under Eu(fod)3 catalysis
    • Dai, W.-M., Wu, A., Lee, M.Y.H. and Lai, K.W. (2001) Neighboring nucleophilic group assisted rearrangement of allylic esters under Eu(fod)3 catalysis. Tetrahedron Letters, 42(25), 4215-4218.
    • (2001) Tetrahedron Letters , vol.42 , Issue.25 , pp. 4215-4218
    • Dai, W.-M.1    Wu, A.2    Lee, M.Y.H.3    Lai, K.W.4
  • 368
    • 0027772649 scopus 로고
    • The enol-keto trigger in initiating arene diradical formation in calicheamicin/esperamicin analogs
    • Semmelhack, M.F., Gallagher, J.J., Minami, T. and Date, T. (1993) The enol-keto trigger in initiating arene diradical formation in calicheamicin/esperamicin analogs. Journal of the American Chemical Society, 115(24), 11618-11619.
    • (1993) Journal of the American Chemical Society , vol.115 , Issue.24 , pp. 11618-11619
    • Semmelhack, M.F.1    Gallagher, J.J.2    Minami, T.3    Date, T.4
  • 370
    • 0032473574 scopus 로고    scopus 로고
    • Actuating cycloaromatization of a bicyclo[7.3.1] enediyne by annelation: an example of inverse dependence on bridge atom hybridization
    • Nantz, M.H., Moss, D.K., Spence, J.D. and Olmstead, M.M. (1998) Actuating cycloaromatization of a bicyclo[7.3.1] enediyne by annelation: an example of inverse dependence on bridge atom hybridization. Angewandte Chemie International Edition, 37(4), 470-473.
    • (1998) Angewandte Chemie International Edition , vol.37 , Issue.4 , pp. 470-473
    • Nantz, M.H.1    Moss, D.K.2    Spence, J.D.3    Olmstead, M.M.4
  • 371
    • 0032554066 scopus 로고    scopus 로고
    • Chemistry of the 2,5-didehydropyridine biradical: computational, kinetic, and trapping studies toward drug design
    • Hoffner, J., Schottelius, M.J., Feichtinger, D. and Chen, P. (1998) Chemistry of the 2,5-didehydropyridine biradical: computational, kinetic, and trapping studies toward drug design. Journal of the American Chemical Society, 120(2), 376-385.
    • (1998) Journal of the American Chemical Society , vol.120 , Issue.2 , pp. 376-385
    • Hoffner, J.1    Schottelius, M.J.2    Feichtinger, D.3    Chen, P.4
  • 372
    • 0030945208 scopus 로고    scopus 로고
    • Synthesis and thermal rearrangement of C, N-dialkynyl imines: a potential aza-Bergman route to 2, 5-didehydropyridine
    • David, W.M. and Kerwin, S.M. (1997) Synthesis and thermal rearrangement of C, N-dialkynyl imines: a potential aza-Bergman route to 2, 5-didehydropyridine. Journal of the American Chemical Society, 119(6), 1464-1465.
    • (1997) Journal of the American Chemical Society , vol.119 , Issue.6 , pp. 1464-1465
    • David, W.M.1    Kerwin, S.M.2
  • 374
    • 42149101354 scopus 로고    scopus 로고
    • Benzofused N-substituted cyclic enediynes: activation and DNA-cleavage potential
    • Basak, A. and Kar, M. (2008) Benzofused N-substituted cyclic enediynes: activation and DNA-cleavage potential. Bioorganic & Medicinal Chemistry, 16(8), 4532-4537.
    • (2008) Bioorganic & Medicinal Chemistry , vol.16 , Issue.8 , pp. 4532-4537
    • Basak, A.1    Kar, M.2
  • 375
    • 84961979252 scopus 로고    scopus 로고
    • C-lysine conjugates: pHcontrolled light-activated reagents for efficient double-stranded DNA cleavage with implications for cancer therapy
    • Yang, W.-Y., Breiner, B., Kovalenko, S.V., et al. (2009) C-lysine conjugates: pHcontrolled light-activated reagents for efficient double-stranded DNA cleavage with implications for cancer therapy. Journal of the American Chemical Society, 131(32), 11458-11470.
    • (2009) Journal of the American Chemical Society , vol.131 , Issue.32 , pp. 11458-11470
    • Yang, W.-Y.1    Breiner, B.2    Kovalenko, S.V.3
  • 377
    • 33645469542 scopus 로고    scopus 로고
    • Synthesis and reactivity of a 9-membered azaenediyne: importance of proximity effect in N-alkylation
    • Roy, S.K. and Basak, A. (2006) Synthesis and reactivity of a 9-membered azaenediyne: importance of proximity effect in N-alkylation. Journal of the Chemical Society, Chemical Communications, (15), 1646-1648.
    • (2006) Journal of the Chemical Society, Chemical Communications , Issue.15 , pp. 1646-1648
    • Roy, S.K.1    Basak, A.2
  • 378
    • 0037161278 scopus 로고    scopus 로고
    • DNA modification by 4-aza-3-ene-1,6-diynes: DNA cleavage, pH-dependent cytosine-specific interactions, and cancer cell cytotoxicity
    • Tuntiwechapikul, W., David, W.M., Kumar, D., Salazar, M. and Kerwin, S.M. (2002) DNA modification by 4-aza-3-ene-1,6-diynes: DNA cleavage, pH-dependent cytosine-specific interactions, and cancer cell cytotoxicity. Biochemistry, 41(16), 5283-5290.
    • (2002) Biochemistry , vol.41 , Issue.16 , pp. 5283-5290
    • Tuntiwechapikul, W.1    David, W.M.2    Kumar, D.3    Salazar, M.4    Kerwin, S.M.5
  • 379
    • 33745049226 scopus 로고    scopus 로고
    • 2-alkynyl-N-propargyl pyridinium salts: pyridinium-based heterocyclic skipped aza-enediynes that cleave DNA by deoxyribosyl hydrogen-atom abstraction and guanine oxidation
    • Tuesuwan, B. and Kerwin, S.M. (2006) 2-alkynyl-N-propargyl pyridinium salts: pyridinium-based heterocyclic skipped aza-enediynes that cleave DNA by deoxyribosyl hydrogen-atom abstraction and guanine oxidation. Biochemistry, 45(23), 7265-7276.
    • (2006) Biochemistry , vol.45 , Issue.23 , pp. 7265-7276
    • Tuesuwan, B.1    Kerwin, S.M.2
  • 380
    • 15944392879 scopus 로고    scopus 로고
    • Dependence of reactivity of a novel 2,6-diamino pyridine-based enediyne on the extent of salt formation with external acids: a possible implication in pH based drug design
    • Basak, A., Kar, M. and Mandal, S. (2005) Dependence of reactivity of a novel 2,6-diamino pyridine-based enediyne on the extent of salt formation with external acids: a possible implication in pH based drug design. Bioorganic & Medicinal Chemistry Letters, 15(8), 2061-2064.
    • (2005) Bioorganic & Medicinal Chemistry Letters , vol.15 , Issue.8 , pp. 2061-2064
    • Basak, A.1    Kar, M.2    Mandal, S.3
  • 381
    • 33748242372 scopus 로고
    • Lactendiynes: a new class of triggered cyclic enediynes
    • Banfi, L. and Guanti, G. (1995) Lactendiynes: a new class of triggered cyclic enediynes. Angewandte Chemie International Edition, 34(21), 2393-2395.
    • (1995) Angewandte Chemie International Edition , vol.34 , Issue.21 , pp. 2393-2395
    • Banfi, L.1    Guanti, G.2
  • 382
    • 0036859322 scopus 로고    scopus 로고
    • Synthesis of intramolecularly activated lactenediynes and evaluation of their activity against plasmid DNA
    • Guanti, G. and Banfi, L. (2002) Synthesis of intramolecularly activated lactenediynes and evaluation of their activity against plasmid DNA. European Journal of Organic Chemistry, (22), 3745-3755.
    • (2002) European Journal of Organic Chemistry , Issue.22 , pp. 3745-3755
    • Guanti, G.1    Banfi, L.2
  • 383
    • 33746507395 scopus 로고    scopus 로고
    • Preparation of optically pure fused polycyclic scaffolds by Ugi reaction followed by olefin and enyne metathesis
    • Basso, A., Banfi, L., Riva, R. and Guanti, G. (2006) Preparation of optically pure fused polycyclic scaffolds by Ugi reaction followed by olefin and enyne metathesis. Tetrahedron, 62(37), 8830-8837.
    • (2006) Tetrahedron , vol.62 , Issue.37 , pp. 8830-8837
    • Basso, A.1    Banfi, L.2    Riva, R.3    Guanti, G.4
  • 384
    • 0037037840 scopus 로고    scopus 로고
    • Synthesis of a new lactenediyne scaffold equipped with three handles
    • Banfi, L. and Guanti, G. (2002) Synthesis of a new lactenediyne scaffold equipped with three handles. Tetrahedron Letters, 43(41), 7427-7429.
    • (2002) Tetrahedron Letters , vol.43 , Issue.41 , pp. 7427-7429
    • Banfi, L.1    Guanti, G.2
  • 385
    • 0037013837 scopus 로고    scopus 로고
    • A carbene insertion route to β-lactam fused cyclic enediynes
    • Basak, A. and Mandal, S. (2002) A carbene insertion route to β-lactam fused cyclic enediynes. Tetrahedron Letters, 43(23), 4241-4243.
    • (2002) Tetrahedron Letters , vol.43 , Issue.23 , pp. 4241-4243
    • Basak, A.1    Mandal, S.2
  • 386
    • 33745830523 scopus 로고    scopus 로고
    • A novel synthesis of β-lactam fused cyclic enediynes by intramolecular Kinugasa reaction
    • Pal, R. and Basak, A. (2006) A novel synthesis of β-lactam fused cyclic enediynes by intramolecular Kinugasa reaction. Journal of the Chemical Society, Chemical Communications, (15), 2992-2994.
    • (2006) Journal of the Chemical Society, Chemical Communications , Issue.15 , pp. 2992-2994
    • Pal, R.1    Basak, A.2
  • 387
    • 3943057458 scopus 로고    scopus 로고
    • L-proline-mediated one-pot synthesis of 3-exomethylene β-lactams via Kinugasa reaction
    • Basak, A. and Ghosh, S.C. (2004) L-proline-mediated one-pot synthesis of 3-exomethylene β-lactams via Kinugasa reaction. Synlett, (9), 1637-1639.
    • (2004) Synlett , Issue.9 , pp. 1637-1639
    • Basak, A.1    Ghosh, S.C.2
  • 388
    • 25444475251 scopus 로고    scopus 로고
    • Intramolecular 1,3-dipolar nitrone cycloaddition route to bicyclic fused enediyne
    • Basak, A. and Ghosh, S.C. (2005) Intramolecular 1,3-dipolar nitrone cycloaddition route to bicyclic fused enediyne. Tetrahedron Letters, 46(43), 7385-7388.
    • (2005) Tetrahedron Letters , vol.46 , Issue.43 , pp. 7385-7388
    • Basak, A.1    Ghosh, S.C.2
  • 389
    • 51149122792 scopus 로고    scopus 로고
    • Synthesis of isoxazoline-fused bicyclic enediynes via intramolecular nitrile oxide-alkene cycloaddition
    • Basak, A. and Pal, R. (2008) Synthesis of isoxazoline-fused bicyclic enediynes via intramolecular nitrile oxide-alkene cycloaddition. Synlett, (14), 2115-2118.
    • (2008) Synlett , Issue.14 , pp. 2115-2118
    • Basak, A.1    Pal, R.2
  • 390
    • 0037459725 scopus 로고    scopus 로고
    • An extremely facile aza-Bergman rearrangement of sterically unencumbered acyclic 3-aza-3-ene-1,5-diynes
    • Feng, L., Kumar, D. and Kerwin, S.M. (2003) An extremely facile aza-Bergman rearrangement of sterically unencumbered acyclic 3-aza-3-ene-1,5-diynes. Journal of Organic Chemistry, 68(6), 2234-2242.
    • (2003) Journal of Organic Chemistry , vol.68 , Issue.6 , pp. 2234-2242
    • Feng, L.1    Kumar, D.2    Kerwin, S.M.3
  • 391
    • 0037459873 scopus 로고    scopus 로고
    • Isolation of a cyclopropane-containing product from the rearrangement of a 3-aza-3-ene-1,5-diyne under acid catalysis
    • Feng, L. and Kerwin, S.M. (2003) Isolation of a cyclopropane-containing product from the rearrangement of a 3-aza-3-ene-1,5-diyne under acid catalysis. Tetrahedron Letters, 44(17), 3463-3466.
    • (2003) Tetrahedron Letters , vol.44 , Issue.17 , pp. 3463-3466
    • Feng, L.1    Kerwin, S.M.2
  • 392
    • 33744770998 scopus 로고    scopus 로고
    • Enediynes from aza-enediynes: C,N-dialkynyl imines undergo both aza-Bergman rearrangement and conversion to enediynes and fumaronitriles
    • Feng, L., Zhang, A. and Kerwin, S.M. (2006) Enediynes from aza-enediynes: C,N-dialkynyl imines undergo both aza-Bergman rearrangement and conversion to enediynes and fumaronitriles. Organic Letters, 8(10), 1983-1986.
    • (2006) Organic Letters , vol.8 , Issue.10 , pp. 1983-1986
    • Feng, L.1    Zhang, A.2    Kerwin, S.M.3
  • 393
    • 0037069725 scopus 로고    scopus 로고
    • Synthesis and thermolysis of heterocyclic 3-aza-3-ene-1,5-diynes
    • Nadipuram, A.K., David, W.M., Kumar, D. and Kerwin, S.M. (2002) Synthesis and thermolysis of heterocyclic 3-aza-3-ene-1,5-diynes. Organic Letters, 4(25), 4543-4546.
    • (2002) Organic Letters , vol.4 , Issue.25 , pp. 4543-4546
    • Nadipuram, A.K.1    David, W.M.2    Kumar, D.3    Kerwin, S.M.4
  • 394
    • 3142660337 scopus 로고    scopus 로고
    • 5H-cyclopentapyrazines from 1,2-dialkynylimidazoles
    • Kerwin, S.M. and Nadipuram, A.K. (2004) 5H-cyclopentapyrazines from 1,2-dialkynylimidazoles. Synlett, (8), 1404-1408.
    • (2004) Synlett , Issue.8 , pp. 1404-1408
    • Kerwin, S.M.1    Nadipuram, A.K.2
  • 395
    • 77949818297 scopus 로고    scopus 로고
    • Cyclization kinetics and biological evaluation of an anticancer 1, 2-dialkynylimidazole
    • Laroche, C., Li, J., Gonzales, C., David, W.M. and Kerwin, S.M. (2010) Cyclization kinetics and biological evaluation of an anticancer 1, 2-dialkynylimidazole. Organic & Biomolecular Chemistry, 8(7), 1535-1539.
    • (2010) Organic & Biomolecular Chemistry , vol.8 , Issue.7 , pp. 1535-1539
    • Laroche, C.1    Li, J.2    Gonzales, C.3    David, W.M.4    Kerwin, S.M.5
  • 396
    • 13244253929 scopus 로고    scopus 로고
    • Photoinduced Bergman cycloaromatization of imidazole-fused enediynes
    • Zhao, Z., Peacock, J.G., Gubler, D.A. and Peterson, M.A. (2005) Photoinduced Bergman cycloaromatization of imidazole-fused enediynes. Tetrahedron Letters, 46(8), 1373-1375.
    • (2005) Tetrahedron Letters , vol.46 , Issue.8 , pp. 1373-1375
    • Zhao, Z.1    Peacock, J.G.2    Gubler, D.A.3    Peterson, M.A.4
  • 397
    • 1842686348 scopus 로고    scopus 로고
    • Bergman cycloaromatization of imidazole-fused enediynes: the remarkable effect of N-aryl substitution
    • Zhao, Z., Peng, Y., Dalley, N.K., Cannon, J.F. and Peterson, M.A. (2004) Bergman cycloaromatization of imidazole-fused enediynes: the remarkable effect of N-aryl substitution. Tetrahedron Letters, 45(18), 3621-3624.
    • (2004) Tetrahedron Letters , vol.45 , Issue.18 , pp. 3621-3624
    • Zhao, Z.1    Peng, Y.2    Dalley, N.K.3    Cannon, J.F.4    Peterson, M.A.5
  • 398
    • 0033553367 scopus 로고    scopus 로고
    • Solvent dependent Bergman cyclization of 2,3-diethynylquinoxaline
    • Kim, C.S. and Russell, K.C. (1999) Solvent dependent Bergman cyclization of 2,3-diethynylquinoxaline. Tetrahedron Letters, 40(20), 3835-3838.
    • (1999) Tetrahedron Letters , vol.40 , Issue.20 , pp. 3835-3838
    • Kim, C.S.1    Russell, K.C.2
  • 399
    • 80051741385 scopus 로고    scopus 로고
    • Synthesis and reactivity of cinnoline-fused cyclic enediyne
    • Vinogradova, O.V., Balova, I.A. and Popik, V.V. (2011) Synthesis and reactivity of cinnoline-fused cyclic enediyne. Journal of Organic Chemistry, 76(16), 6937-6941.
    • (2011) Journal of Organic Chemistry , vol.76 , Issue.16 , pp. 6937-6941
    • Vinogradova, O.V.1    Balova, I.A.2    Popik, V.V.3
  • 400
    • 78650678610 scopus 로고    scopus 로고
    • Richter cyclization and co-cyclization reactions of triazene-masked diazonium ions
    • Goeminne, A., Scammells, P.J., Devine, S.M. and Flynn, B.L. (2010) Richter cyclization and co-cyclization reactions of triazene-masked diazonium ions. Tetrahedron Letters, 51(52), 6882-6885.
    • (2010) Tetrahedron Letters , vol.51 , Issue.52 , pp. 6882-6885
    • Goeminne, A.1    Scammells, P.J.2    Devine, S.M.3    Flynn, B.L.4
  • 402
    • 0347600556 scopus 로고    scopus 로고
    • Synthesis and thermal cyclization of an enediynesulfonamide
    • Klein, M. and Konig, B. (2004) Synthesis and thermal cyclization of an enediynesulfonamide. Tetrahedron, 60(5), 1087-1092.
    • (2004) Tetrahedron , vol.60 , Issue.5 , pp. 1087-1092
    • Klein, M.1    Konig, B.2
  • 404
    • 35048877547 scopus 로고    scopus 로고
    • Synthesis and unusual reactivity of NTosyl-4,5-benzoazacyclodeca-2,6-diyne, yneamino-containing enediyne
    • Poloukhtine, A. and Popik, V.V. (2007) Synthesis and unusual reactivity of NTosyl-4,5-benzoazacyclodeca-2,6-diyne, yneamino-containing enediyne. Journal of the American Chemical Society, 129(40), 12062-12063.
    • (2007) Journal of the American Chemical Society , vol.129 , Issue.40 , pp. 12062-12063
    • Poloukhtine, A.1    Popik, V.V.2
  • 406
    • 0042990949 scopus 로고    scopus 로고
    • Changing the reactivity of enediynes by metal-ion coordination
    • Konig, B. (2000) Changing the reactivity of enediynes by metal-ion coordination. European Journal of Organic Chemistry, (3), 381-385.
    • (2000) European Journal of Organic Chemistry , Issue.3 , pp. 381-385
    • Konig, B.1
  • 407
    • 11244309015 scopus 로고    scopus 로고
    • Activation of macrocyclic enediynes by transannular cyclization
    • Basak, A., Roy, S.K. and Mandal, S. (2005) Activation of macrocyclic enediynes by transannular cyclization. Angewandte Chemie International Edition, 44(1), 132-135.
    • (2005) Angewandte Chemie International Edition , vol.44 , Issue.1 , pp. 132-135
    • Basak, A.1    Roy, S.K.2    Mandal, S.3
  • 408
    • 33750499739 scopus 로고    scopus 로고
    • Synthesis and thermal reactivity of pyrrolidine-and 2-pyrrolidinone-fused cyclic enediynes
    • Roy, P.B. and Basak, A. (2006) Synthesis and thermal reactivity of pyrrolidine-and 2-pyrrolidinone-fused cyclic enediynes. Synlett, (17), 2804-2806.
    • (2006) Synlett , Issue.17 , pp. 2804-2806
    • Roy, P.B.1    Basak, A.2
  • 409
    • 28044465982 scopus 로고    scopus 로고
    • Synthesis and protein degradation capacity of photoactivated enediynes
    • Fouad, F.S., Wright, J.M., Plourde II, G., et al. (2005) Synthesis and protein degradation capacity of photoactivated enediynes. Journal of Organic Chemistry, 70(24), 9789-9797.
    • (2005) Journal of Organic Chemistry , vol.70 , Issue.24 , pp. 9789-9797
    • Fouad, F.S.1    Wright, J.M.2    Plourde, G.3
  • 410
    • 77956512884 scopus 로고    scopus 로고
    • Bergman cyclization of acyclic amino acid derived enediynes leads to the formation of 2,3-dihydrobenzo[f]isoindoles
    • Gredicak, M., Matanovic, I., Zimmermann, B. and Jeric, I. (2010) Bergman cyclization of acyclic amino acid derived enediynes leads to the formation of 2,3-dihydrobenzo[f]isoindoles. Journal of Organic Chemistry, 75(18), 6219-6228.
    • (2010) Journal of Organic Chemistry , vol.75 , Issue.18 , pp. 6219-6228
    • Gredicak, M.1    Matanovic, I.2    Zimmermann, B.3    Jeric, I.4
  • 411
  • 412
    • 33751370328 scopus 로고    scopus 로고
    • New unsaturated azamacrocyclic enediynes: synthesis, structural analysis and thermal behavior
    • Gonzalez, I., Roglans, A., Benet-Buchholz, J. and Rourac, P. (2006) New unsaturated azamacrocyclic enediynes: synthesis, structural analysis and thermal behavior. Synlett, (18), 3041-3044.
    • (2006) Synlett , Issue.18 , pp. 3041-3044
    • Gonzalez, I.1    Roglans, A.2    Benet-Buchholz, J.3    Rourac, P.4
  • 413
    • 12344289470 scopus 로고    scopus 로고
    • Computational studies on the cyclizations of enediynes, enyne-allenes, and related polyunsaturated systems
    • Schreiner, P.R., Navarro-Vazques, A. and Prall, M. (2005) Computational studies on the cyclizations of enediynes, enyne-allenes, and related polyunsaturated systems. Accounts of Chemical Research, 38(1), 29-37.
    • (2005) Accounts of Chemical Research , vol.38 , Issue.1 , pp. 29-37
    • Schreiner, P.R.1    Navarro-Vazques, A.2    Prall, M.3
  • 414
    • 0011041531 scopus 로고
    • Synthesis and photoinduced cis-trans isomerization of diaryl enediyne chromophores
    • Konig, B., Schofield, E., Bubenitschek, P. and Jones, P.G. (1994) Synthesis and photoinduced cis-trans isomerization of diaryl enediyne chromophores. Journal of Organic Chemistry, 59(23), 7142-7143.
    • (1994) Journal of Organic Chemistry , vol.59 , Issue.23 , pp. 7142-7143
    • Konig, B.1    Schofield, E.2    Bubenitschek, P.3    Jones, P.G.4
  • 415
    • 0029150062 scopus 로고
    • Controlled acceleration and Inhibition of Bergman cyclization by metal chlorides
    • Warner, B.P., Miller, S.P., Broene, R.D. and Buchwald, S.L. (1995) Controlled acceleration and Inhibition of Bergman cyclization by metal chlorides. Science 269(5225), 814-816.
    • (1995) Science , vol.269 , Issue.5225 , pp. 814-816
    • Warner, B.P.1    Miller, S.P.2    Broene, R.D.3    Buchwald, S.L.4
  • 416
    • 0004512579 scopus 로고    scopus 로고
    • Synthesis and metal ion binding studies of enediyne-containing crown ethers
    • McPhee, M.M. and Kerwin, S.M. (1996) Synthesis and metal ion binding studies of enediyne-containing crown ethers. Journal of Organic Chemistry, 61(26), 9385-9393.
    • (1996) Journal of Organic Chemistry , vol.61 , Issue.26 , pp. 9385-9393
    • McPhee, M.M.1    Kerwin, S.M.2
  • 417
    • 0004462514 scopus 로고
    • Huthing & Werf Verlag, Basel, Switzerland
    • Elias, H.-G. (1990) Macromolekule, vol. 1, Huthing & Werf Verlag, Basel, Switzerland, p. 817.
    • (1990) Macromolekule , vol.1 , pp. 817
    • Elias, H.-G.1
  • 418
    • 74849135034 scopus 로고    scopus 로고
    • Synthesis of novel "rod-coil" brush polymers with conjugated backbones through Bergman cyclization
    • Cheng, X., Ma, J., Zhi, J., Yang, X. and Hu, A. (2010) Synthesis of novel "rod-coil" brush polymers with conjugated backbones through Bergman cyclization. Macromolecules, 43(2), 909-913.
    • (2010) Macromolecules , vol.43 , Issue.2 , pp. 909-913
    • Cheng, X.1    Ma, J.2    Zhi, J.3    Yang, X.4    Hu, A.5
  • 419
    • 84985645263 scopus 로고
    • Highly unsaturated oligomeric hydrocarbons-α-(phenylethynyl)-ω-phenylpoly[1,2-phenylene (2,1-ethynediyl)]
    • Grubbs, R.H. and Kratz, D. (1993) Highly unsaturated oligomeric hydrocarbons-α-(phenylethynyl)-ω-phenylpoly[1,2-phenylene (2,1-ethynediyl)]. Chemische Berichte, 126(1), 149-157.
    • (1993) Chemische Berichte , vol.126 , Issue.1 , pp. 149-157
    • Grubbs, R.H.1    Kratz, D.2
  • 421
    • 0029928040 scopus 로고    scopus 로고
    • Synthesis of macrocyclic enediynes by twofold C-alkylation
    • Konig, B., Pitsch, W., Dix, I. and Jones, P.G. (1996) Synthesis of macrocyclic enediynes by twofold C-alkylation. Synthesis, (4), 446-448.
    • (1996) Synthesis , Issue.4 , pp. 446-448
    • Konig, B.1    Pitsch, W.2    Dix, I.3    Jones, P.G.4
  • 424
    • 0032492937 scopus 로고    scopus 로고
    • Synthesis and thermal reactivity of a novel macrocyclic enediynes and its copper(II) complex
    • Basak, A. and Shain, J.C. (1998) Synthesis and thermal reactivity of a novel macrocyclic enediynes and its copper(II) complex. Tetrahedron Letters, 39(19), 3029-3030.
    • (1998) Tetrahedron Letters , vol.39 , Issue.19 , pp. 3029-3030
    • Basak, A.1    Shain, J.C.2
  • 425
    • 0032546311 scopus 로고    scopus 로고
    • Synthesis and thermal behaviour of a novel diazaenediyne and its copper(II)-complex
    • Basak, A. and Shain, J.C. (1998) Synthesis and thermal behaviour of a novel diazaenediyne and its copper(II)-complex. Tetrahedron Letters, 39(12), 1623-1624.
    • (1998) Tetrahedron Letters , vol.39 , Issue.12 , pp. 1623-1624
    • Basak, A.1    Shain, J.C.2
  • 426
    • 0033590486 scopus 로고    scopus 로고
    • 1,8-Diazabicyclo[6.6.6]eicosa-4,11,17-triyne: a flexible cage for protons, copper(I) and silver(I)
    • Kunze, A., Gleiter, R. and Rominger, F. (1999) 1,8-Diazabicyclo[6.6.6]eicosa-4,11,17-triyne: a flexible cage for protons, copper(I) and silver(I). Journal of the Chemical Society, Chemical Communications, (2), 171-172.
    • (1999) Journal of the Chemical Society, Chemical Communications , Issue.2 , pp. 171-172
    • Kunze, A.1    Gleiter, R.2    Rominger, F.3
  • 427
    • 0035802169 scopus 로고    scopus 로고
    • Mg2+-induced thermal enediyne cyclization at ambient temperature
    • Rawat, D.S. and Zaleski, J.M. (2001) Mg2+-induced thermal enediyne cyclization at ambient temperature. Journal of the American Chemical Society, 123(39), 9675-9676.
    • (2001) Journal of the American Chemical Society , vol.123 , Issue.39 , pp. 9675-9676
    • Rawat, D.S.1    Zaleski, J.M.2
  • 429
    • 0034601631 scopus 로고    scopus 로고
    • Synthesis and thermal reactivity of a novel bissalicylaldimino enediyne and its Cu(II) and Ni(II) complexes
    • Basak, A. and Rudra, K.R. (2000) Synthesis and thermal reactivity of a novel bissalicylaldimino enediyne and its Cu(II) and Ni(II) complexes. Tetrahedron Letters, 41(37), 7231-7234.
    • (2000) Tetrahedron Letters , vol.41 , Issue.37 , pp. 7231-7234
    • Basak, A.1    Rudra, K.R.2
  • 431
    • 0034596351 scopus 로고    scopus 로고
    • Metalloenediynes: ligand field control of thermal Bergman cyclization reactions
    • Benites, P.J., Rawat, D.S. and Zaleski, J.M. (2000) Metalloenediynes: ligand field control of thermal Bergman cyclization reactions. Journal of the American Chemical Society, 122(30), 7208-7217.
    • (2000) Journal of the American Chemical Society , vol.122 , Issue.30 , pp. 7208-7217
    • Benites, P.J.1    Rawat, D.S.2    Zaleski, J.M.3
  • 432
    • 0037500108 scopus 로고    scopus 로고
    • Metal-ligand chargetransfer-promoted photoelectronic Bergman cyclization of copper metalloenediynes: photochemical DNA cleavage via C-4'H-atom abstraction
    • Benites, P.J., Holmberg, P.C., Rawat, D.S., et al. (2003). Metal-ligand chargetransfer-promoted photoelectronic Bergman cyclization of copper metalloenediynes: photochemical DNA cleavage via C-4'H-atom abstraction. Journal of the American Chemical Society, 125(21), 6334-6346.
    • (2003) Journal of the American Chemical Society , vol.125 , Issue.21 , pp. 6334-6346
    • Benites, P.J.1    Holmberg, P.C.2    Rawat, D.S.3
  • 433
    • 0141629816 scopus 로고    scopus 로고
    • Photochemistry of diethynyl sulfides: a cycloaromatization for the formation of five-membered rings
    • Lewis, K.D., Wenzler, D.I. and Matzger, A.J. (2003) Photochemistry of diethynyl sulfides: a cycloaromatization for the formation of five-membered rings. Organic Letters, 5(13), 2195-2197.
    • (2003) Organic Letters , vol.5 , Issue.13 , pp. 2195-2197
    • Lewis, K.D.1    Wenzler, D.I.2    Matzger, A.J.3
  • 434
    • 3342875706 scopus 로고    scopus 로고
    • Ethynyl sulfides as participants in cascade cycloaromatizations
    • Lewis, K.D., Rowe, M.P. and Matzger, A.J. (2004) Ethynyl sulfides as participants in cascade cycloaromatizations. Tetrahedron, 60(34), 7191-7196.
    • (2004) Tetrahedron , vol.60 , Issue.34 , pp. 7191-7196
    • Lewis, K.D.1    Rowe, M.P.2    Matzger, A.J.3
  • 435
    • 0035478821 scopus 로고    scopus 로고
    • Substituent effects on the Bergman cyclization of (Z)-1,5-hexadiyne-3-enes: a systematic computational study
    • Prall, M., Wittkopp, A., Fokin, A.A. and Schreiner, P.R. (2001) Substituent effects on the Bergman cyclization of (Z)-1,5-hexadiyne-3-enes: a systematic computational study. Journal of Computational Chemistry, 22(13), 1605-1614.
    • (2001) Journal of Computational Chemistry , vol.22 , Issue.13 , pp. 1605-1614
    • Prall, M.1    Wittkopp, A.2    Fokin, A.A.3    Schreiner, P.R.4
  • 436
    • 0344666656 scopus 로고    scopus 로고
    • Effect of ring fusion on the electronic absorption and emission properties of oligothiophenes
    • Zhang, X. and Matzger, A.J. (2003) Effect of ring fusion on the electronic absorption and emission properties of oligothiophenes. Journal of Organic Chemistry, 68(25), 9813-9815.
    • (2003) Journal of Organic Chemistry , vol.68 , Issue.25 , pp. 9813-9815
    • Zhang, X.1    Matzger, A.J.2
  • 437
    • 13244275128 scopus 로고    scopus 로고
    • A unique approach to metal-induced Bergman cyclization: long-range enediyne activation by ligand-to-metal charge transfer
    • Bhattacharyya, S., Pink, M., Baik, M.H. and Zaleski, J.M. (2005) A unique approach to metal-induced Bergman cyclization: long-range enediyne activation by ligand-to-metal charge transfer. Angewandte Chemie International Edition, 44(4), 592-595.
    • (2005) Angewandte Chemie International Edition , vol.44 , Issue.4 , pp. 592-595
    • Bhattacharyya, S.1    Pink, M.2    Baik, M.H.3    Zaleski, J.M.4
  • 438
    • 77955125855 scopus 로고    scopus 로고
    • Cycloadditions and cyclizations of acetylenic, allenic, and conjugated dienyl sulfones
    • Back, T.G., Clary, K.N. and Gao, D. (2010) Cycloadditions and cyclizations of acetylenic, allenic, and conjugated dienyl sulfones. Chemical Reviews, 110(8), 4498-4553.
    • (2010) Chemical Reviews , vol.110 , Issue.8 , pp. 4498-4553
    • Back, T.G.1    Clary, K.N.2    Gao, D.3
  • 439
    • 0038306205 scopus 로고    scopus 로고
    • Synthesis, reactions and DNA damaging abilities of 10-membered enediynesulfone and related compounds
    • Suzuki, I., Shigenaga, A., Manabe, A., Nemoto, H. and Masayuki, S. (2003) Synthesis, reactions and DNA damaging abilities of 10-membered enediynesulfone and related compounds. Tetrahedron, 59(30), 5691-5704.
    • (2003) Tetrahedron , vol.59 , Issue.30 , pp. 5691-5704
    • Suzuki, I.1    Shigenaga, A.2    Manabe, A.3    Nemoto, H.4    Masayuki, S.5
  • 443
    • 0032524185 scopus 로고    scopus 로고
    • Generation of biradicals and subsequent formation of quinolines and 5H-benzo[b]carbazoles fromN-[2-(1-alkynyl)phenyl]ketenimines
    • Shi, C. and Wang, K.K. (1998) Generation of biradicals and subsequent formation of quinolines and 5H-benzo[b]carbazoles fromN-[2-(1-alkynyl)phenyl]ketenimines. Journal of Organic Chemistry, 63(10), 3517-3520.
    • (1998) Journal of Organic Chemistry , vol.63 , Issue.10 , pp. 3517-3520
    • Shi, C.1    Wang, K.K.2
  • 444
    • 0037662089 scopus 로고    scopus 로고
    • Cascade cyclizations via N, 4-didehydro-2-(phenylamino)pyridine biradicals/zwitterions generated from enynecarbodiimides
    • Li, H., Petersen, J.L. and Wang, K.K. (2003) Cascade cyclizations via N, 4-didehydro-2-(phenylamino)pyridine biradicals/zwitterions generated from enynecarbodiimides. Journal of Organic Chemistry, 68(14), 5512-5518.
    • (2003) Journal of Organic Chemistry , vol.68 , Issue.14 , pp. 5512-5518
    • Li, H.1    Petersen, J.L.2    Wang, K.K.3
  • 445
    • 3042781836 scopus 로고    scopus 로고
    • Biradicals/zwitterions from thermolysis of enyne-isocyanates application to the synthesis of 2(1H)-pyridones, benzofuro[3, 2-c]pyridin-1(2H)-ones, 2,5-dihydro-1H-pyrido[4,3-b]indol-1-ones, and related compounds
    • Li, H., Yang, H., Petersen, J.L. and Wang, K.K. (2004) Biradicals/zwitterions from thermolysis of enyne-isocyanates. application to the synthesis of 2(1H)-pyridones, benzofuro[3, 2-c]pyridin-1(2H)-ones, 2,5-dihydro-1H-pyrido[4,3-b]indol-1-ones, and related compounds. Journal of Organic Chemistry, 69(13), 4500-4508.
    • (2004) Journal of Organic Chemistry , vol.69 , Issue.13 , pp. 4500-4508
    • Li, H.1    Yang, H.2    Petersen, J.L.3    Wang, K.K.4
  • 446
    • 34548779742 scopus 로고    scopus 로고
    • Charakterisierung nichtstatistischer dynamischer effekte in der cyclisierung von eninallenen mittels kinetischer isotopeneffekte
    • Schmittel, M., Vavilala, C. and Jaquet, R. (2007) Charakterisierung nichtstatistischer dynamischer effekte in der cyclisierung von eninallenen mittels kinetischer isotopeneffekte. Angewandte Chemie International Edition, 46(36), 6911-6914.
    • (2007) Angewandte Chemie International Edition , vol.46 , Issue.36 , pp. 6911-6914
    • Schmittel, M.1    Vavilala, C.2    Jaquet, R.3
  • 447
    • 0001647738 scopus 로고    scopus 로고
    • Thermolysis of 2-(3-phenylsulfonylprop-1-ynyl)benzonitrile: an aza-Myers type cyclization to isoquinolines
    • Wu, M.-J., Lin, C.-F., Chen, S.-H. and Lee, F.-C. (1999) Thermolysis of 2-(3-phenylsulfonylprop-1-ynyl)benzonitrile: an aza-Myers type cyclization to isoquinolines. Journal of the Chemical Society, Perkin Transactions 1, (20), 2875-2876.
    • (1999) Journal of the Chemical Society, Perkin Transactions , vol.1 , Issue.20 , pp. 2875-2876
    • Wu, M.-J.1    Lin, C.-F.2    Chen, S.-H.3    Lee, F.-C.4
  • 448
    • 26844480670 scopus 로고    scopus 로고
    • Myers-Saito and Schmittel cyclizations of enyne-(hetero)-1,2,3-trienes: a DFT study on the structure-reactivity relationship
    • Lu, Y.-X., Zou, J.-W., Wang, H.-Q. and Yu, Q.-S. (2005) Myers-Saito and Schmittel cyclizations of enyne-(hetero)-1,2,3-trienes: a DFT study on the structure-reactivity relationship. Journal of Molecular Structure: THEOCHEM., 732(1-3), 233-238.
    • (2005) Journal of Molecular Structure: THEOCHEM. , vol.732 , Issue.1-3 , pp. 233-238
    • Lu, Y.-X.1    Zou, J.-W.2    Wang, H.-Q.3    Yu, Q.-S.4
  • 449
    • 0035887151 scopus 로고    scopus 로고
    • Synthesis of cyclo-1, 3-dien-5-ynes
    • Hopf, H. and Kruger, A. (2001) Synthesis of cyclo-1, 3-dien-5-ynes. Chemistry-A European Journal, 7(20), 4378-4386.
    • (2001) Chemistry-A European Journal , vol.7 , Issue.20 , pp. 4378-4386
    • Hopf, H.1    Kruger, A.2
  • 450
    • 65549089790 scopus 로고    scopus 로고
    • Aza Hopf cyclization: synthesis and reactivity of cyclic azadieneynes
    • Mandal, S. and Basak, A. (2009) Aza Hopf cyclization: synthesis and reactivity of cyclic azadieneynes. Tetrahedron Letters, 50(26), 3641-3644.
    • (2009) Tetrahedron Letters , vol.50 , Issue.26 , pp. 3641-3644
    • Mandal, S.1    Basak, A.2
  • 452
    • 0032544307 scopus 로고    scopus 로고
    • Two novel thermal biradical cyclizations in theory and experiment: new synthetic routes to 6H-indolo[2,3-b]quinolines and 2-aminoquinolines from enyne-carbodiimides
    • Schmittel, M., Steffen, J.-P., Engels, B., Lennartz, C. and Hanrath, M. (1998) Two novel thermal biradical cyclizations in theory and experiment: new synthetic routes to 6H-indolo[2,3-b]quinolines and 2-aminoquinolines from enyne-carbodiimides. Angewandte Chemie International Edition, 37(17), 2371-2373.
    • (1998) Angewandte Chemie International Edition , vol.37 , Issue.17 , pp. 2371-2373
    • Schmittel, M.1    Steffen, J.-P.2    Engels, B.3    Lennartz, C.4    Hanrath, M.5
  • 453
    • 0942300606 scopus 로고    scopus 로고
    • Modular three-component solid-phase synthesis of unsymmetrical guanidines via resin capture of carbodiimides
    • Boguszewski, P.A., Rahman, S.S. and Ganesan, A. (2004) Modular three-component solid-phase synthesis of unsymmetrical guanidines via resin capture of carbodiimides. Journal of Combinatorial Science, 6(1), 32-34.
    • (2004) Journal of Combinatorial Science , vol.6 , Issue.1 , pp. 32-34
    • Boguszewski, P.A.1    Rahman, S.S.2    Ganesan, A.3
  • 457
    • 0037181077 scopus 로고    scopus 로고
    • On the regioselectivity of the cyclization of enyne-ketenes: a computational investigation and comparison with the Myers-Saito and Schmittel reaction
    • Masch, P.W., Remenyi, C., Helten, H. and Engels, B. (2002) On the regioselectivity of the cyclization of enyne-ketenes: a computational investigation and comparison with the Myers-Saito and Schmittel reaction. Journal of the American Chemical Society, 124(8), 1823-1828.
    • (2002) Journal of the American Chemical Society , vol.124 , Issue.8 , pp. 1823-1828
    • Masch, P.W.1    Remenyi, C.2    Helten, H.3    Engels, B.4
  • 458
    • 0034930473 scopus 로고    scopus 로고
    • Trifluoroacetyl-2-trimethylstannyl-and 1-trifluoroacetyl-2-bromoacetylenes as new dienophiles in the Diels-Alder reactions
    • Koldobskii, A.B., Shilova, O.S. and Kalinin, V.N. (2011) Trifluoroacetyl-2-trimethylstannyl-and 1-trifluoroacetyl-2-bromoacetylenes as new dienophiles in the Diels-Alder reactions. Mendeleev Communications, (11), 99-100.
    • (2011) Mendeleev Communications , Issue.11 , pp. 99-100
    • Koldobskii, A.B.1    Shilova, O.S.2    Kalinin, V.N.3
  • 459
    • 49349097984 scopus 로고    scopus 로고
    • Synthesis and unusual [2+2]-cycloaddition reactions of ethyl 2-chloro-2-oxobut-3-ynoates with unactivated alkenes
    • Koldobskii, A.B., Solodova, E.V., Godovikov, I.A. and Kalinin, V.N. (2008) Synthesis and unusual [2+2]-cycloaddition reactions of ethyl 2-chloro-2-oxobut-3-ynoates with unactivated alkenes. Tetrahedron, 64(40), 9555-9560.
    • (2008) Tetrahedron , vol.64 , Issue.40 , pp. 9555-9560
    • Koldobskii, A.B.1    Solodova, E.V.2    Godovikov, I.A.3    Kalinin, V.N.4
  • 460
    • 44649145762 scopus 로고    scopus 로고
    • Perfluoroacetylenephosphonates in Diels-Alder reactions: synthesis of perfluoroalkylated heterocyclic and carbocyclic phosphonates
    • Tverdomed, S.N., Roeschenthaler, G.-V., Kalinovich, N., Lork, E., Dogadina, A.V. and Ionin, B.I. (2008) Perfluoroacetylenephosphonates in Diels-Alder reactions: synthesis of perfluoroalkylated heterocyclic and carbocyclic phosphonates. Journal of Fluorine Chemistry, 129(6), 478-485.
    • (2008) Journal of Fluorine Chemistry , vol.129 , Issue.6 , pp. 478-485
    • Tverdomed, S.N.1    Roeschenthaler, G.-V.2    Kalinovich, N.3    Lork, E.4    Dogadina, A.V.5    Ionin, B.I.6
  • 461
    • 0002479422 scopus 로고
    • Arbuzov rearrangement with the participation of fluoro-, chloro-, bromo-and iodo-acetylenes
    • Zhurnal Obshchei Khimii, 35(11), 1917-1921
    • Ionin, B.I. and Petrov, A.A. (1965) Arbuzov rearrangement with the participation of fluoro-, chloro-, bromo-and iodo-acetylenes. Russian Journal of General Chemistry, 35(11), 1917-1921; Zhurnal Obshchei Khimii, 35(11), 1917-1921.
    • (1965) Russian Journal of General Chemistry , vol.35 , Issue.11 , pp. 1917-1921
    • Ionin, B.I.1    Petrov, A.A.2
  • 462
    • 1442290773 scopus 로고    scopus 로고
    • CRC Press, Boka Raton, London, New York, Washington, D.C.
    • Savignac, P. and Iorga, B. (2003) Modern Phosphonate Chemistry, CRC Press, Boka Raton, London, New York, Washington, D.C., p. 552.
    • (2003) Modern Phosphonate Chemistry , pp. 552
    • Savignac, P.1    Iorga, B.2
  • 463
    • 33747475482 scopus 로고    scopus 로고
    • A methodology for synthesis of primary o-phenylenebisphosphines and o-Chlorophenylphosphines
    • Zhurnal Obshchei Khimii, 76(6), 925-934
    • Tverdomed, S.N., Dogadina, A.V. and Ionin, B.I. (2006) A methodology for synthesis of primary o-phenylenebisphosphines and o-Chlorophenylphosphines. Russian Journal of General Chemistry, 76(6), 885-894; Zhurnal Obshchei Khimii, 76(6), 925-934.
    • (2006) Russian Journal of General Chemistry , vol.76 , Issue.6 , pp. 885-894
    • Tverdomed, S.N.1    Dogadina, A.V.2    Ionin, B.I.3
  • 464
    • 0037492125 scopus 로고    scopus 로고
    • New method of synthesis of phosphinobenzenes and 1,2-diphosphinobenzenes
    • Zhurnal Obshchei Khimii, 73(2), 343-344
    • Tverdomed, S.N., Dogadina, A.V. and Ionin, B.I. (2003) New method of synthesis of phosphinobenzenes and 1,2-diphosphinobenzenes. Russian Journal of General Chemistry, 73(2), 319-320; Zhurnal Obshchei Khimii, 73(2), 343-344.
    • (2003) Russian Journal of General Chemistry , vol.73 , Issue.2 , pp. 319-320
    • Tverdomed, S.N.1    Dogadina, A.V.2    Ionin, B.I.3
  • 465
    • 84863702904 scopus 로고    scopus 로고
    • Synthesis of brominesubstituted cyclohexenylphosphonates
    • Zhurnal Obshchei Khimii, 82(4), 566-569
    • Titov, K.S., Svintsitskaya, N.I. and Ionin, B.I. (2012) Synthesis of brominesubstituted cyclohexenylphosphonates. Russian Journal of General Chemistry, 82(4), 652-654; Zhurnal Obshchei Khimii, 82(4), 566-569.
    • (2012) Russian Journal of General Chemistry , vol.82 , Issue.4 , pp. 652-654
    • Titov, K.S.1    Svintsitskaya, N.I.2    Ionin, B.I.3
  • 466
    • 84868353581 scopus 로고    scopus 로고
    • Epoxidation of cyclohexa-1,4-dienylphosphonates
    • Zhurnal Obshchei Khimii, 82(8), 1400-1402
    • Titov, K.S., Svintsitskaya, N.I. and Ionin, B.I. (2012) Epoxidation of cyclohexa-1,4-dienylphosphonates. Russian Journal of General Chemistry, 82(8), 1461-1463; Zhurnal Obshchei Khimii, 82(8), 1400-1402.
    • (2012) Russian Journal of General Chemistry , vol.82 , Issue.8 , pp. 1461-1463
    • Titov, K.S.1    Svintsitskaya, N.I.2    Ionin, B.I.3
  • 468
    • 84858449286 scopus 로고    scopus 로고
    • Synthesis of dialkyl(aryl)cyclobutenylphosphine oxides
    • Bogachenkov, A.S., Efremova, M.M. and Ionin, B.I. (2012) Synthesis of dialkyl(aryl)cyclobutenylphosphine oxides. Tetrahedron Letters, 53(16), 2100-2102.
    • (2012) Tetrahedron Letters , vol.53 , Issue.16 , pp. 2100-2102
    • Bogachenkov, A.S.1    Efremova, M.M.2    Ionin, B.I.3
  • 469
    • 85026240340 scopus 로고    scopus 로고
    • Formation of 3-diphenylphosphorylpyrroles in consecutive reactions of dibromocyclobutenyldiphenylphosphine oxides with aniline
    • (accepted for publication).
    • Bogachenkov, A.S., Ionin, B.I. and Röschenthaler, G.-V. (2012) Formation of 3-diphenylphosphorylpyrroles in consecutive reactions of dibromocyclobutenyldiphenylphosphine oxides with aniline. Tetrahedron Letters, (accepted for publication).
    • (2012) Tetrahedron Letters
    • Bogachenkov, A.S.1    Ionin, B.I.2    Röschenthaler, G.-V.3
  • 470
    • 3242751325 scopus 로고    scopus 로고
    • Metal complex catalysis in a synthesis of pyridine bases
    • Dzhemilev, U.M., Selimov, F.A. and Tolstikov, G.A. (2001) Metal complex catalysis in a synthesis of pyridine bases. ARKIVOC, (9), 85-116.
    • (2001) ARKIVOC , Issue.9 , pp. 85-116
    • Dzhemilev, U.M.1    Selimov, F.A.2    Tolstikov, G.A.3
  • 471
    • 77949605231 scopus 로고    scopus 로고
    • New methodology of heterocyclization: the electrophilic addition reactions of selenium di-and tetrahalides and tellurium tetrachloride to diethynyl silanes and germanes
    • Amosova, S.V. and Martynov, A.V. (2010) New methodology of heterocyclization: the electrophilic addition reactions of selenium di-and tetrahalides and tellurium tetrachloride to diethynyl silanes and germanes. Mini-Reviews in Organic Chemistry, 7(1), 23-32.
    • (2010) Mini-Reviews in Organic Chemistry , vol.7 , Issue.1 , pp. 23-32
    • Amosova, S.V.1    Martynov, A.V.2
  • 472
    • 0036096076 scopus 로고    scopus 로고
    • Synthesis and properties of acetylenic derivatives of pyrazoles
    • ed. A.R. Katritzky), Elsevier, New York-London
    • Vasilevsky, S.F., Tretyakov, E.V. and Elguero, J. (2002) Synthesis and properties of acetylenic derivatives of pyrazoles, in Advances in Heterocyclic Chemistry, vol. 82 (ed. A.R. Katritzky), Elsevier, New York-London, pp. 1-99.
    • (2002) Advances in Heterocyclic Chemistry , vol.82 , pp. 1-99
    • Vasilevsky, S.F.1    Tretyakov, E.V.2    Elguero, J.3
  • 473
    • 19544362859 scopus 로고    scopus 로고
    • Unexpected results in the heterocyclization of 5-acetylenylpyrazole-4-carboxylic acid hydrazides under the influence of CuCl: formation of diazepinones and dehydrodimerization into the corresponding bis(pyrazolo[4,3-d][1,2]diazepinones)
    • Vasilevsky, S.F., Mshvidobadze, E.V., Mamatyuk, V.I., Romanenko, G.V. and Elguero, J. (2005) Unexpected results in the heterocyclization of 5-acetylenylpyrazole-4-carboxylic acid hydrazides under the influence of CuCl: formation of diazepinones and dehydrodimerization into the corresponding bis(pyrazolo[4,3-d][1,2]diazepinones). Tetrahedron Letters, 46, 4457-4459.
    • (2005) Tetrahedron Letters , vol.46 , pp. 4457-4459
    • Vasilevsky, S.F.1    Mshvidobadze, E.V.2    Mamatyuk, V.I.3    Romanenko, G.V.4    Elguero, J.5
  • 474
    • 70350705891 scopus 로고    scopus 로고
    • Competition between 5-exo and 6-endo-dig anionic cyclizations of hydrazides of o-acetylenyl benzoic acids and based-catalyzed fragmentation/recyclization of the initial 5-exodig products
    • Vasilevsky, S.F., Mikhailovskaya, T.F., Mamatyuk, V.I. et al. (2009) Competition between 5-exo and 6-endo-dig anionic cyclizations of hydrazides of o-acetylenyl benzoic acids and based-catalyzed fragmentation/recyclization of the initial 5-exodig products. Journal of Organic Chemistry, 74, 8106-8117.
    • (2009) Journal of Organic Chemistry , vol.74 , pp. 8106-8117
    • Vasilevsky, S.F.1    Mikhailovskaya, T.F.2    Mamatyuk, V.I.3
  • 475
    • 78650139535 scopus 로고    scopus 로고
    • Addition reactions of 1,1,1-trifluoro-4-trimethylstannylbut-3-yn-2-one and 1,1,1-trifluorobut-3-yn-2-one to some tetrahydropyridines. Synthesis of trifluoroacylated polysubstituted tetrahydroazocines. Russian Chemical
    • Izvestiya Akademii Nauk. Seriya Khimicheskaya, 60(5), 988-991; ChemInform, 2011, 42(17)
    • Koldobskii, A.B., Solodova, E.V. and Kalinin, V.N. (2011) Addition reactions of 1,1,1-trifluoro-4-trimethylstannylbut-3-yn-2-one and 1,1,1-trifluorobut-3-yn-2-one to some tetrahydropyridines. Synthesis of trifluoroacylated polysubstituted tetrahydroazocines. Russian Chemical. Bulletin, 60(5), 1010-1013; Izvestiya Akademii Nauk. Seriya Khimicheskaya, 60(5), 988-991; ChemInform, 2011, 42(17), doi: 10.1002/chin.201117177
    • (2011) Bulletin , vol.60 , Issue.5 , pp. 1010-1013
    • Koldobskii, A.B.1    Solodova, E.V.2    Kalinin, V.N.3
  • 476
    • 51049092976 scopus 로고    scopus 로고
    • Ag-mediated reactions: coupling and heterocyclization reactions
    • Weibel, J.-M., Blanc, A. and Pale, P. (2008) Ag-mediated reactions: coupling and heterocyclization reactions. Chemical Reviews, 108, 3149-3173.
    • (2008) Chemical Reviews , vol.108 , pp. 3149-3173
    • Weibel, J.-M.1    Blanc, A.2    Pale, P.3
  • 477
    • 79951629063 scopus 로고    scopus 로고
    • Rhodium-catalyzed tandem heterocyclization and carbonylative [(3+2)+1] cyclization of diyne-enones
    • Zhao, W. and Zhang, J. (2011). Rhodium-catalyzed tandem heterocyclization and carbonylative [(3+2)+1] cyclization of diyne-enones. Organic Letters, 13(4), 688-691.
    • (2011) Organic Letters , vol.13 , Issue.4 , pp. 688-691
    • Zhao, W.1    Zhang, J.2
  • 478
    • 33845247117 scopus 로고    scopus 로고
    • Gold and platinum catalysis of enyne cycloisomerization
    • Zhang, L., Sun, J. and Kozmin, S.A. (2006) Gold and platinum catalysis of enyne cycloisomerization. Advanced Synthesis & Catalysis, 348, 2271-2296.
    • (2006) Advanced Synthesis & Catalysis , vol.348 , pp. 2271-2296
    • Zhang, L.1    Sun, J.2    Kozmin, S.A.3
  • 479
    • 84863691346 scopus 로고    scopus 로고
    • Heterocyclization reaction of chloroacetylenephosphonates with 2-acylamidomalonates into 5-(dialkoxyphosphorylmethylidene)oxazolines
    • Zhurnal Obshchei Khimii, 82(4), 694-696
    • Khramchikhin, V.A., Dogadina, A.V., Khramchikhin, A.V. and Ionin, B.I. (2012) Heterocyclization reaction of chloroacetylenephosphonates with 2-acylamidomalonates into 5-(dialkoxyphosphorylmethylidene)oxazolines. Russian Journal of General Chemistry, 82(4), 776-778; Zhurnal Obshchei Khimii, 82(4), 694-696.
    • (2012) Russian Journal of General Chemistry , vol.82 , Issue.4 , pp. 776-778
    • Khramchikhin, V.A.1    Dogadina, A.V.2    Khramchikhin, A.V.3    Ionin, B.I.4
  • 480
    • 84864039954 scopus 로고    scopus 로고
    • Highly regioselective heterocyclization reactions of 1H-1,2,4-triazole-3-thiols with chloroacetylenephosphonates
    • Erkhitueva, E.B., Dogadina, A.V., Khramchikhin, A.V. and Ioni, B.I. (2012) Highly regioselective heterocyclization reactions of 1H-1,2,4-triazole-3-thiols with chloroacetylenephosphonates. Tetrahedron Letters, 53(33), 4304-4308.
    • (2012) Tetrahedron Letters , vol.53 , Issue.33 , pp. 4304-4308
    • Erkhitueva, E.B.1    Dogadina, A.V.2    Khramchikhin, A.V.3    Ioni, B.I.4
  • 481
    • 84860193226 scopus 로고    scopus 로고
    • A comprehensive history of arynes in natural product total synthesis
    • Tadross, P.M. and Stoltz, B.M. (2012) A comprehensive history of arynes in natural product total synthesis. Chemical Reviews, 112(6), 3550-3577.
    • (2012) Chemical Reviews , vol.112 , Issue.6 , pp. 3550-3577
    • Tadross, P.M.1    Stoltz, B.M.2
  • 483
    • 33746933488 scopus 로고    scopus 로고
    • Enediyne isomers of tetraethynylethene
    • Bowling, N.P. and McMahon, R.J. (2006) Enediyne isomers of tetraethynylethene. Journal of Organic Chemistry, 71(16), 5841-5847.
    • (2006) Journal of Organic Chemistry , vol.71 , Issue.16 , pp. 5841-5847
    • Bowling, N.P.1    McMahon, R.J.2
  • 484
    • 20144379689 scopus 로고    scopus 로고
    • Conjugated oligoenynes based on the diethynylethene unit
    • Nielsen, M.B. and Diederich, F. (2005) Conjugated oligoenynes based on the diethynylethene unit. Chemical Reviews, 105(5), 1837-1868.
    • (2005) Chemical Reviews , vol.105 , Issue.5 , pp. 1837-1868
    • Nielsen, M.B.1    Diederich, F.2
  • 485
    • 33947727055 scopus 로고    scopus 로고
    • The Sonogashira reaction: a booming methodology in synthetic organic chemistry
    • Chinchilla, R. and Najera, C. (2007) The Sonogashira reaction: a booming methodology in synthetic organic chemistry. Chemical Reviews, 107(3), 874-922.
    • (2007) Chemical Reviews , vol.107 , Issue.3 , pp. 874-922
    • Chinchilla, R.1    Najera, C.2
  • 486
    • 70349204174 scopus 로고    scopus 로고
    • Creation of Stabilized electrochromic materials by taking advantage of azulene skeletons
    • Ito, S. and Morita, N. (2009) Creation of Stabilized electrochromic materials by taking advantage of azulene skeletons. European Journal of Organic Chemistry, (27), 4567-4579.
    • (2009) European Journal of Organic Chemistry , Issue.27 , pp. 4567-4579
    • Ito, S.1    Morita, N.2
  • 487
    • 64549103746 scopus 로고    scopus 로고
    • Synthesis and redox behavior of ene-diyne scaffolds that bear ferrocenes at the periphery
    • Shoji, T., Ito, S., Toyota, K. and Morita, N. (2009) Synthesis and redox behavior of ene-diyne scaffolds that bear ferrocenes at the periphery. Tetrahedron Letters, 50(23), 2825-2827.
    • (2009) Tetrahedron Letters , vol.50 , Issue.23 , pp. 2825-2827
    • Shoji, T.1    Ito, S.2    Toyota, K.3    Morita, N.4
  • 488
    • 70450172331 scopus 로고    scopus 로고
    • Towards the preparation of electrochromic materials with strong absorption in the near-infrared region: synthesis and redox behavior of azulene-substituted enediyne scaffolds connected by a 9,10-anthracenediyl spacer
    • Ito, S., Iida, T., Kawakami, J., Okujima, T. and Morita, N. (2009) Towards the preparation of electrochromic materials with strong absorption in the near-infrared region: synthesis and redox behavior of azulene-substituted enediyne scaffolds connected by a 9,10-anthracenediyl spacer. European Journal of Organic Chemistry, (31), 5355-5364.
    • (2009) European Journal of Organic Chemistry , Issue.31 , pp. 5355-5364
    • Ito, S.1    Iida, T.2    Kawakami, J.3    Okujima, T.4    Morita, N.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.